House Dust Mite Injection

Dosage Form: injection
Allergenic Extracts For Diagnostic Use Only

ALLERGENIC EXTRACTS, FOR DIAGNOSTIC USE ONLY

DIRECTIONS FOR USE

DESCRIPTION

Sterile diagnostic extracts are supplied in either phenol-saline diluent for Intradermal Testing or in diluent containing glycerin 50% (v/v) for Percutaneous Testing and phenol 0.4% (preservative). Inactive ingredients may include: sodium chloride for isotonicity, glycerin, and sodium bicarbonate as a buffer. Inactive ingredients in mold extracts may include residual potassium phosphate, and calcium carbonate from growth media.

Pollens are individually extracted from pure pollen extracted in a phenol-preserved sodium bicarbonate solution. Short Ragweed and Mixed (Tall and Short) Ragweed extracts are standardized by Antigen E content and so labeled. The Antigen E content of extracts containing Short Ragweed at a concentration more dilute than a weight/volume ratio of 1:10 are obtained by calculating the Antigen E content based on the assay value of more concentrated extract. Pollen extracts are filtered aseptically and after final packaging, they are tested for sterility and safety.

House Dust, a heterogenous, widely distributed allergen, is among the most frequently encountered as a primary or accompanying cause of allergic symptoms. Allergic inhalants found in house dust include mites, insects, mold spores, feathers, animal dander, pollens, hairs, food and cleansing agent residues. Individual environs may contain certain items not ordinarily found so that a stock house dust extract may not elicit a response on testing. House Dust Extracts are prepared from dust collected from homes and from establishments which clean household rugs. It is extracted from buffered, aqueous extracting fluid. House Dust Extract is dialyzed, filtered aseptically, and after final packaging is tested for sterility and safety.

Molds (fungi) are present in all inhabited places at all seasons of the year; they are so ubiquitous that they are prevalent at times when common allergic pollens and other inhalants are not. In the home and surroundings, molds are found in upholstered furniture, mattresses, drapes, cellar and storage room dust, woolens, leather goods, fruits, meats, cheeses, garden soil and on plants. Spores, mycelial fragments and mold residues are thus inhaled, contacted and ingested continuously. Mold extracts are extracted in a phenol preserved saline solution. The extract is dialyzed, filtered aseptically and after final packaging is tested for sterility and safety.

Foods, miscellaneous inhalants and epidermals are individually extracted in phenol preserved saline, filtered aseptically and after final packaging are tested for sterility and safety.

CLINICAL PHARMACOLOGY

Diagnostically (for skin testing), the allergen combines with IgE antibodies fixed to mast cells in the skin. This complexing causes an increase in cellular permeability and degranulation of the mast cells releasing chemical mediators. These mediators (such as histamine) are responsible for a local inflammatory response of wheal and erythema typical of a positive skin test reaction and also, the symptoms commonly associated with allergic disease.1 The more mediator release, the larger the reaction (wheal and erythema).

INDICATIONS AND USAGE

These products are for diagnostic use only. Diagnostic allergenic extracts are indicated for use in skin testing to establish the clinical relevance of specific allergens to which the patient has been exposed. By measuring skin test response the physician may assess the degree of sensitivity that patients have to the allergens. For extracts standardized in AU and BAU, see individual directions for use.  Allergenic extracts for diagnostic use only of coffee, mosquito, cottonseed, and flaxseed have not been shown by adequate data to be safe and effective for therapeutic use.

CONTRAINDICATIONS

Patients on beta blockers can be non-responsive to beta agonists that may be required to reverse a systemic reaction (also, see boxed WARNINGS statement and ADVERSE REACTIONS). The physician should carefully weigh the benefit derived from skin testing vs. the risk to the patient should a systemic reaction arise.

Patients with unstable asthma or steroid dependent asthmatics and patients with underlying cardiovascular disease are at greater risk to a fatal outcome from a systemic allergic reaction2, 3. See also PRECAUTIONS and ADVERSE REACTIONS.

WARNINGS

Patients should always be observed for at least 20 - 30 minutes after skin testing. In the event of a marked systemic reaction such as urticaria, angioedema, wheezing, dyspnea, respiratory obstruction, hypotension, coma and death (see ADVERSE REACTIONS), applications of a tourniquet above the injection site and administration of 0.2 mL to 1 mL (0.01 mg/kg) of epinephrine injection (1:1,000) are recommended. Maximal recommended dose for children between 2 and 12 years of age is 0.5 mL. The tourniquet is then gradually released at 15 minute intervals. Patients under treatment with beta blockers may be refractory to the usual dose of epinephrine.

Volume expanders and vasopressor agents may be required to reverse hypotension, inhalation bronchodilators and parenteral aminophylline may be required to reverse bronchospasm. In case of respiratory obstruction, oxygen and intubation may be necessary. Life-threatening reactions unresponsive to the above may require cardiopulmonary resuscitation.

PRECAUTIONS

INFORMATION FOR PATIENTS:

Patients should be instructed to describe any active allergic symptoms such as rhinitis, wheezing, dyspnea, etc. prior to testing. Also, see ADVERSE REACTIONS and WARNINGS Sections.

Patients should always be observed 20 to 30 minutes after testing.

General:

1. In the presence of active symptoms such as rhinitis, wheezing, dyspnea, etc., the indications for skin testing must be weighed carefully against the risk of temporarily aggravating the symptoms by the testing itself. Objective assessment of pulmonary function such as Peak Expiratory Flow Rate (PEFR) before allergen administration and prior to discharge may be useful in unstable asthmatics to reduce the chances of exacerbation of the patient’s asthma. Patients should be instructed to describe any active allergic symptoms as described above prior to skin testing and encouraged to report any late reactions from this testing. Also, see ADVERSE REACTIONS and WARNINGS sections.
   
2. Store allergenic extracts between 2o - 8o C at all times, even during use.
   
3. Care must be taken to avoid drawing blood.
   1. For percutaneous testing, if blood is observed, immediately wipe the allergen from the site.
      
   2. For intradermal skin testing, pull gently on the syringe plunger and note if any blood enters the syringe. If blood is obtained, reposition the needle and repeat before injecting (see DOSAGE AND ADMINISTRATION).
   
   
4. Allergenic extracts become less potent with age. Allergenic extracts containing glycerin 50% v/v are relatively stable. Non-glycerinated aqueous extracts, particularly dilute forms as used for intradermal skin testing, have been shown to be extremely unstable. Until such time as stability studies are complete with dilute allergens, new intradermal strength materials should be prepared every few weeks.
   
5. Use standard aseptic precautions if making dilutions from stock concentrates to intradermal strength.
   
6. For intradermal testing: Extracts in glycerin 50% v/v must be diluted with a non-glycerinated diluent and must be diluted at least 25-fold to less than 2% glycerin by volume, as glycerin above this level can cause false positive intradermal skin test results.

PREGNANCY - CATEGORY C:

Animal reproduction studies have not been conducted with allergenic extracts. It is also not known whether allergenic extracts can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity.

Controlled studies of hyposensitization with moderate to high doses of allergenic extracts during conception and all trimesters of pregnancy have failed to demonstrate any risk to the fetus or to the mother4. However, on the basis of histamine's known ability to contract the uterine muscle, the release of significant amounts of histamine from allergen exposure to skin test overdose should be avoided on theoretical grounds. Therefore, allergenic extracts should be used cautiously in a pregnant woman and only if clearly needed.

Pediatric Use:

Allergenic extracts for diagnostic use have been given safely in infants and young children. Infants have lower skin test reactivity to histamine, as well as common allergens. Skin test reactivity gradually increases to age 6 and plateaus to age 60. Therefore, small skin test reactions should be anticipated in children under age 6.

Geriatric Use:

Skin test reactivity gradually decreases after age 60. Therefore, smaller skin test reactions should be anticipated in adults over age 60.

Nursing Mothers:

It is not known if allergens administered subcutaneously appear in human milk. Because many drugs are excreted in human milk, caution should be exercised when allergenic extracts are administered to a nursing woman.

Carcinogenesis, mutagenesis, impairment of fertility:

Studies in animals have not been performed.

Drug Interactions:

Drugs can interfere with the performance of skin tests5.

Antihistamines: Response to mediator (histamine) released by allergens is suppressed by antihistamines. The length of suppression varies and is dependent on individual patient, type of antihistamine and length of time the patient has been on antihistamines. The duration of this suppression may be as little as 24 hours (chlorpheniramine), and can be as long as 40 days (astemizole).

      Tricyclic Antidepressants: These exert a potent and sustained decrease of skin reactivity to histamine which may last for a few weeks.

      Beta2 Agonists: Oral terbutaline and parenteral ephedrine, in general, have been shown to decrease allergen induced wheal.

      Dopamine: Intravenous infusion of dopamine may inhibit skin test responses.

      Beta Blocking Agents: Propanolol can significantly increase skin test reactivity.

      Other Drugs: Short acting steroids, inhaled beta2 agonists, theophylline and cromolyn do not seem to affect skin test response.

ADVERSE REACTIONS

Fatalities from skin testing in the United States have been extensively reviewed by Lockey.2 Six fatalities were associated with intradermal testing without previous percutaneous testing and one was associated with a combination of percutaneous (scratch) and intradermal skin testing. With careful attention to dosage and administration, fatal reactions occur infrequently, but it must be remembered that allergenic extracts are highly potent to sensitive individuals and overdosage could result in anaphylactic symptoms. Therefore it is imperative that physicians administering allergenic extracts for skin testing understand, and be prepared for the treatment of severe reactions.

Local: Immediate wheal and erythema reactions are to be expected; but if very large, may be the first manifestation of a systemic reaction. In such cases, immediately wipe the test site(s) with sterile gauze or cotton to remove excess allergen.

Systemic Reactions: Systemic reactions are characterized by one or more of the following symptoms: sneezing, mild to severe generalized urticaria, itching (other than at the skin test site), extensive or generalized edema, wheezing, asthma, dyspnea, cyanosis, hypotension, syncope, and upper airway obstruction. Symptoms may progress to shock and death. Patients should always be observed for at least 20 - 30 minutes after testing.

Volume expanders and vasopressor agents may be required to reverse hypotension. Inhalational bronchodilators and parenteral aminophylline may be required to reverse bronchospasm. Severe airway obstruction unresponsive to bronchodilator may require tracheal intubation and use of oxygen. In the event of a marked systemic reaction, application of a tourniquet above the injection site and the administration of 0.02 mL to 1.0 mL of epinephrine injection (1:1,000) is recommended. Maximum recommended dose for children between 2 and 12 years of age is 0.3 mL. The tourniquet should not be left in place without loosening for 90 seconds every 15 minutes.

Adverse events should be reported via MedWatch (1-800-FDA-1088). Adverse experience Reporting, HFM-210 Center for Biologics Evaluation & Research, Food and Drug Administration, 1401 Rockville Pike, Rockville, MD 20852-1448.

OVERDOSAGE

Signs and symptoms of overdose are typically large local and systemic reactions. For management of overdose reactions, refer to the ADVERSE REACTIONS section above.

DOSAGE AND ADMINISTRATION

Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.

Skin test techniques for immediate (Type I) hypersensitivity testing fall into two major categories: percutaneous, and intracutaneous.

Percutaneous techniques: For percutaneous testing, in general, skin is scratched, punctured or pricked just before the allergen is applied or through a drop of test allergen. There are several devices available for this technique. Refer to the manufacturer or distributor's circular for specific directions for their use.

In General:

1. It is recommended that the test areas should be placed no closer than 4 - 5 cm apart to avoid interference of reactions when several tests are applied.
   
2. Skin test areas should be cleansed with alcohol and air dried.
   
3. Preferably, the allergen should be placed on the volar surface of the forearm, upper arm, or the patient's back. The patient should be placed in a comfortable position prior to testing.
   
4. For scratch testing, a sharp, clean, sterile instrument is used to abrade the skin, but not to draw blood. Each scratch should be about 2 - 4 mm in length. A small drop of extract is placed on the surface of the skin.
   
5. Prick testing: For prick testing, a sharp, sterile instrument is used to puncture the skin slightly, applying it at a 15 - 20o angle to the skin. The instrument is gently raised, "tenting” the skin until it pops out, generally pricking through the drop of allergen. Do not draw blood.
   
6. For puncture testing, a sharp, clean, sterile instrument must be used. Puncture the skin, through the drop of allergen, perpendicular to the skin. Do not draw blood.

For all of the above techniques, a separate instrument must be used for each patient; if the instrument is to be used to pass through the allergen, to avoid cross-contamination, a separate instrument is to be used for each allergen. The test should be read in 15 minutes, measuring both wheal size and erythema.

Intracutaneous (intradermal) testing: General: Intradermal testing is more sensitive than percutaneous testing and its specificity is dependent on dose. Intradermal testing is not intended as an initial screen unless used in highly dilute solutions. Intradermal testing is usually reserved for allergens that have demonstrated either negative or equivocal percutaneous skin test response in the face of positive or unclear history.

Intradermal testing of one allergen in several serial dilutions (beginning with the weakest to the more concentrated dilutions) may also be useful in assessing degree of patient sensitivity for the establishment of a safe starting dose for immunotherapy.

Bulk extracts must be diluted for intradermal testing. Use of Sterile Diluent for Allergenic Extracts or Sterile Diluent for Allergenic Extracts Normal Saline with HSA (albumin saline) is recommended. Dilutions should be made with sterile disposable syringes using aseptic technique. Commonly, 10 fold dilutions are used to achieve a desired concentration for intradermal testing and continuation of immunotherapy. For example, transferring 0.5 mL of a 10,000 PNU/mL extract into 4.5 mL of diluent will yield 5 mL of extract at 1,000 PNU/mL. For weight volume products, a 1:100 w/v dilution may be prepared from a 1:10 w/v by transferring 0.5 mL of the 1:10 w/v to 4.5 mL of diluent. Prepare as many additional serial dilutions as necessary to reach the appropriate concentration. As a general rule intradermal strength should begin at no higher than 1/100 to 1/1000 of the percutaneous strength that resulted in a negative skin test reaction.

1. It is recommended that the test areas should be spaced no less than 5 cm apart to avoid interference with adjacent allergen or control.
   
2. Skin should be cleansed with alcohol and air dried.
   
3. A sterile 1 mL or ½ mL syringe with a 26 - 30 gauge needle should be used. A separate sterile syringe should be used for each extract and each patient.
   
4. Care should be taken to eliminate air bubbles from the syringe prior to injecting the test dose. It is suggested that not more than 6 - 10 allergens of each different type be used at any one time. Very sensitive patients may show rapid response.
   
5. The skin is held tensely, and the needle is inserted almost parallel to the skin, beveled side up far enough to cover the beveled portion. Slowly inject sufficient extract to make a small bleb of approximately 5 mm in diameter (0.01 - 0.02 mL).
   
6. Read the test results in 15 minutes.

Selection of the proper strength for intracutaneous testing: A general rule for the prevention of untoward reactions, particularly in extremely sensitive patients, is to screen by percutaneous methods initially, and begin intradermal testing at a strength not more than 1/100 of a negative or equivocal percutaneous reaction.

Controls: In both percutaneous and intracutaneous tests, a negative control test with diluent alone should be performed because some patients exhibit dermographia, and/or other non-specific irritant responses.

As a positive control in the evaluation of allergenic skin testing, histamine 1 mg/mL (histamine base) should be used for percutaneous testing, and histamine 0.1 mg/mL (histamine base) should be used for intradermal testing.

Interpretation of results: Patient's response is graded on the basis of the size of erythema or wheal.6 General guidelines follow for percutaneous testing, different devices and/or techniques influence the size of the reaction, therefore it is important to refer to the device manufacturer's or distributor's instructions when grading reactions.

Percutaneous (prick or scratch) test:

0	No reaction or less than control.
+	Erythema greater than control, smaller than a nickel (21 mm diameter).
++	Erythema greater than a nickel in diameter, no wheal.
+++	Wheal and erythema without pseudopods.
++++	Wheal and erythema with pseudopods.

Intradermal test:

0	No reaction or less than negative control.
+	3-4 mm wheal with erythema, or erythema alone larger than a nickel (21 mm diamether).
++	4-8 mm wheal and erythema, without pseudopods.
+++	Over 8 mm wheal and erythema without pseudopods
++++	Wheal and erythema with pseudopods.

HOW SUPPLIED

For scratch and prick testing: 5 mL dropper applicator vials in 50% v/v glycerin. Available individually and in a complete set of the most common allergens. Available in either Protein Nitrogen Units (PNU/mL) or weight to volume (w/v).

For intracutaneous testing: 5 mL sterile vials, aqueous based, individually and in a complete set of the most common allergens. Available in either Protein Nitrogen Units (PNU/mL) or weight to volume (w/v).

HistatrolR Positive skin test control - histamine. 1 mg/mL and 0.1 mg/mL histamine base.

See Product Catalog for specific diagnostic concentrations available.

STORAGE

To maintain stability of allergenic extracts, proper storage conditions are essential. Bulk concentrates and diluted extracts are to be stored at 2o to 8o C even during use. Bulk or diluted extracts are not to be frozen. Do not use after the expiration date shown on the vial label.

REFERENCES

1. Holgate, S.T., Robinson, C. and Church, M.K., Mediators of immediate hypersensitivity. In Middleton et al: Allergy Principles and Practice, St. Louis, 1988, C.V. Mosby, p 135.
   
2. Lockey, R.F., et al, Fatalities from immunotherapy (IT) and skin testing (ST). J. Allergy Clin. Immunol., 1987:79:660.
   
3. Reid, M.J. et al.  Survey of fatalities from skin testing and immunotherapy. 1985-1989. J. Allergy Clin Immunol. 1993; 92:6.
   
4. DeBuske L. M. et al.  Special problems regarding Allergen Immunotherapy in Immunology and Allergy Clinics of North America. Greenburger, P.A. Ed. February 1992; 145-149.
   
5. Bousquet, J. In vivo methods for the study of allergy: skin test, techniques and interpretation. In: Middleton et al.: Allergy Principles and Practice 3rd Ed. St. Louis: DV Mosby, 1988:167.
   
6. Freedman, S.O., Asthma and Allergic Rhinitis II. Clinical Aspects, in Freedman and Gold Clinical Immunology 2nd Ed. New York: Harper & Row, 1976:131.

Revision: June 2002

©ALK-Abello, Inc.                                                 112N

Distributed in Canada by:

Western Allergy Services, LTD.

121-6154 Westminister Highway

Richmond, B.C. V7C404

HOUSE DUST  house dust  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6000 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOUSE DUST (HOUSE DUST) HOUSE DUST 10000 [PNU]  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6000-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ALMOND  almond food  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6100 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALMOND (ALMOND) ALMOND 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6100-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

APPLE  apple food  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6101 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength APPLE (APPLE) APPLE 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6101-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

APRICOT  apricot  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6102 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength APRICOT (APRICOT) APRICOT 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6102-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ASPARAGUS  asparagus  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6103 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ASPARAGUS (ASPARAGUS) ASPARAGUS 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6103-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

AVOCADO  avocado  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6104 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOCADO (AVOCADO) AVOCADO 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6104-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

BANANA  banana  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6105 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BANANA (BANANA) BANANA 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6105-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

BARLEY  barley food  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6106 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BARLEY (BARLEY) BARLEY 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6106-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

BEAN  pinto bean kidney bean  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6107 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BEAN (BEAN) BEAN 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6107-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

STRING BEAN  string bean green bean  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6108 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength STRING BEAN (STRING BEAN) STRING BEAN 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6108-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

BEEF  beef  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6109 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BEEF (BEEF) BEEF 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6109-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

BRAZIL NUT  brazil nut  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6110 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BRAZIL NUT (BRAZIL NUT) BRAZIL NUT 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6110-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

BROCCOLI  broccoli  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6112 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BROCCOLI (BROCCOLI) BROCCOLI 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6112-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

BUCKWHEAT  buckwheat  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6113 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BUCKWHEAT (BUCKWHEAT) BUCKWHEAT 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6113-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CABBAGE  cabbage  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6114 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CABBAGE (CABBAGE) CABBAGE 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6114-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CANTALOUPE  cantaloupe  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6115 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CANTALOUPE (CANTALOUPE) CANTALOUPE 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6115-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CARROT  carrot  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6116 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CARROT (CARROT) CARROT 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6116-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CASEIN  casein  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6118 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CASEIN (CASEIN) CASEIN 0.01 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6118-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CELERY  celery  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6120 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CELERY (CELERY) CELERY 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6120-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CHERRY  cherry  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6121 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHERRY (CHERRY) CHERRY 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6121-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CHICKEN  chicken meat  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6122 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHICKEN (CHICKEN) CHICKEN 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6122-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CINNAMON  cinnamon  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6123 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CINNAMON (CINNAMON) CINNAMON 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6123-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CLAM  clam  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6124 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CLAM (CLAM) CLAM 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6124-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

COCOA BEAN  cocoa bean whole bean chocolate  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6125 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength COCOA BEAN (COCOA BEAN) COCOA BEAN 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6125-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

COCONUT  coconut  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6127 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength COCONUT (COCONUT) COCONUT 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6127-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CODFISH  codfish  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6128 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CODFISH (CODFISH) CODFISH 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6128-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

COFFEE BEAN  coffee  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6129 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength COFFEE BEAN (COFFEE BEAN) COFFEE BEAN 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6129-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CRAB  crab  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6130 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CRAB (CRAB) CRAB 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6130-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CUCUMBER  cucumber  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6132 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CUCUMBER (CUCUMBER) CUCUMBER 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6132-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

EGG WHITE  egg white  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6133 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength EGG WHITE (EGG WHITE) EGG WHITE 0.01 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6133-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

EGG  whole egg  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6135 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength EGG (EGG) EGG 0.01 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6135-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

EGG YOLK  egg yolk  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6136 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength EGG YOLK (EGG YOLK) EGG YOLK 0.01 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6136-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

FLOUNDER  flounder  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6137 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength FLOUNDER (FLOUNDER) FLOUNDER 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6137-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

GARLIC  garlic  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6138 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GARLIC (GARLIC) GARLIC 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6138-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

GRAPE  white seedless grape  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6139 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GRAPE (GRAPE) GRAPE 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6139-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

GRAPEFRUIT  grapefruit  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6141 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GRAPEFRUIT (GRAPEFRUIT) GRAPEFRUIT 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6141-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

KARAYA GUM  karaya gum bassora  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6143 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength KARAYA GUM (KARAYA GUM) KARAYA GUM 0.005 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6143-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

HONEYDEW MELON  honeydew  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6146 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HONEYDEW MELON (HONEYDEW MELON) HONEYDEW MELON 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6146-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

LAMB  lamb  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6149 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LAMB (LAMB) LAMB 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6149-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

LEMON  lemon  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6170 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LEMON (LEMON) LEMON 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6170-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

LETTUCE  lettuce  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6171 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LETTUCE (LETTUCE) LETTUCE 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6171-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

LIMA BEAN  lima bean  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6173 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIMA BEAN (LIMA BEAN) LIMA BEAN 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6173-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

LOBSTER  lobster  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6174 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LOBSTER (LOBSTER) LOBSTER 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6174-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

GOAT MILK  goat milk  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6177 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GOAT MILK (GOAT MILK) GOAT MILK 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6177-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

COW MILK  milk whole cows  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6178 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength COW MILK (COW MILK) COW MILK 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6178-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

MUSHROOM  mushroom agaricus spp  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6180 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CULTIVATED MUSHROOM (CULTIVATED MUSHROOM) CULTIVATED MUSHROOM 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6180-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

MUSTARD SEED  mustard seed  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6181 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MUSTARD SEED (MUSTARD SEED) MUSTARD SEED 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6181-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

OAT  oat grain  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6183 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OAT (OAT) OAT 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6183-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

BLACK OLIVE  olive  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6185 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BLACK OLIVE (BLACK OLIVE) BLACK OLIVE 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6185-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ONION  onion  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6186 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ONION (ONION) ONION 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6186-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ORANGE  orange  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6187 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ORANGE (ORANGE) ORANGE 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6187-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

OYSTER  oyster  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6189 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OYSTER (OYSTER) OYSTER 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6189-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PEA  green pea english  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6191 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PEA (PEA) PEA 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6191-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PEACH  peach  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6192 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PEACH (PEACH) PEACH 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6192-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PEANUT  peanut  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6193 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PEANUT (PEANUT) PEANUT 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6193-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PEAR  pear  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6195 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PEAR (PEAR) PEAR 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6195-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PECAN  pecan  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6196 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PECAN (PECAN) PECAN 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6196-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

GREEN BELL PEPPER  bell  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6197 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GREEN BELL PEPPER (GREEN BELL PEPPER) GREEN BELL PEPPER 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6197-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

BLACK PEPPER  black pepper  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6198 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BLACK PEPPER (BLACK PEPPER) BLACK PEPPER 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6198-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PINEAPPLE  pineapple  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6200 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PINEAPPLE (PINEAPPLE) PINEAPPLE 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6200-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PISTACHIO  pistachio nut  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6202 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PISTACHIO (PISTACHIO) PISTACHIO 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6202-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PLUM  plum  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6203 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PLUM (PLUM) PLUM 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6203-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PORK  pork  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6204 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PORK (PORK) PORK 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6204-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

POTATO  sweet potato  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6205 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POTATO (POTATO) POTATO 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6205-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

POTATO  white potato  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6206 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POTATO (POTATO) POTATO 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6206-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

RICE  rice  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6208 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RICE (RICE) RICE 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6208-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

RYE  rye  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6210 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RYE (RYE) RYE 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6210-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

SALMON  salmon  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6212 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALMON (SALMON) SALMON 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6212-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

SESAME SEED  sesame seed  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6213 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SESAME SEED (SESAME SEED) SESAME SEED 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6213-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

SHRIMP  shrimp  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6214 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SHRIMP (SHRIMP) SHRIMP 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6214-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

SOYBEAN  soybean  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6216 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SOYBEAN (SOYBEAN) SOYBEAN 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6216-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

SPINACH  spinach  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6218 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SPINACH (SPINACH) SPINACH 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6218-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

SQUASH  squash  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6219 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SQUASH (SQUASH) SQUASH 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6219-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

STRAWBERRY  strawberry  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6220 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength STRAWBERRY (STRAWBERRY) STRAWBERRY 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6220-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CORN  sweet corn  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6221 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CORN (CORN) CORN 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6221-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

TOMATO  tomato  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6224 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TOMATO (TOMATO) TOMATO 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6224-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

TUNA  tuna  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6226 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TUNA (TUNA) TUNA 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6226-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

TURKEY  turkey meat  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6229 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TURKEY (TURKEY) TURKEY 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6229-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

VANILLA  vanilla  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6230 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength VANILLA (VANILLA) VANILLA 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6230-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ENGLISH WALNUT  english walnut  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6231 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ENGLISH WALNUT (ENGLISH WALNUT) ENGLISH WALNUT 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6231-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

WATERMELON  watermelon  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6233 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength WATERMELON (WATERMELON) WATERMELON 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6233-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

WHEAT  whole wheat wheat grain  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6234 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength WHEAT (WHEAT) WHEAT 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6234-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

BOS TAURUS SKIN  cattle epithelium  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6300 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BOS TAURUS SKIN (BOS TAURUS SKIN) BOS TAURUS SKIN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6300-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

COTTON FIBER  cattle epithelium  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6302 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength COTTON FIBER (COTTON FIBER) COTTON FIBER 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6302-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

COTTON SEED  cottonseed  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6304 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength COTTON SEED (COTTON SEED) COTTON SEED 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6304-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CANIS LUPUS FAMILIARIS SKIN  dog epithelium  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6306 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CANIS LUPUS FAMILIARIS SKIN (CANIS LUPUS FAMILIARIS SKIN) CANIS LUPUS FAMILIARIS SKIN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6306-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CAVIA PORCELLUS SKIN  guinea pig epithelium  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6309 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CAVIA PORCELLUS SKIN (CAVIA PORCELLUS SKIN) CAVIA PORCELLUS SKIN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6309-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

EQUUS CABALLUS SKIN  horse epithelium  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6311 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength EQUUS CABALLUS SKIN (EQUUS CABALLUS SKIN) EQUUS CABALLUS SKIN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6311-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CEIBA PENTANDRA FIBER  kapok  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6312 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CEIBA PENTANDRA FIBER (CEIBA PENTANDRA FIBER) CEIBA PENTANDRA FIBER 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6312-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

MUS MUSCULUS SKIN  mouse epithelium  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6314 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MUS MUSCULUS SKIN (MUS MUSCULUS SKIN) MUS MUSCULUS SKIN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6314-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ORRIS  orris root  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6317 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ORRIS (ORRIS) ORRIS 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6317-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PYRETHRUM CINERARIIFOLIUM  pyrethrum  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6318 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PYRETHRUM CINERARIIFOLIUM (PYRETHRUM CINERARIIFOLIUM) PYRETHRUM CINERARIIFOLIUM 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6318-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

RABBIT  rabbit epithelium  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6320 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RABBIT (RABBIT) RABBIT 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6320-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

SOLENOPSIS INVICTA  fire ant  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6400 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SOLENOPSIS INVICTA (SOLENOPSIS INVICTA) SOLENOPSIS INVICTA 0.01 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6400-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PERIPLANETA AMERICANA  american cockroach  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6403 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PERIPLANETA AMERICANA (PERIPLANETA AMERICANA) PERIPLANETA AMERICANA 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6403-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

BLATELLA GERMANICA  german cockroach  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6405 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BLATELLA GERMANICA (BLATELLA GERMANICA) BLATELLA GERMANICA 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6405-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ACREMONIUM STRICTUM  acremonium strictum  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6500 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACREMONIUM STRICTUM (ACREMONIUM STRICTUM) ACREMONIUM STRICTUM 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6500-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ALTERNARIA TENUIS  alternaria tenuis a alternata  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6502 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALTERNARIA ALTERNATA (ALTERNARIA ALTERNATA) ALTERNARIA ALTERNATA 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6502-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ASPERGILLUS FUMIGATUS  aspergillus fumigatus  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6504 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ASPERGILLUS FUMIGATUS (ASPERGILLUS FUMIGATUS) ASPERGILLUS FUMIGATUS 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6504-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ASPERGILLUS NIGER VAR NIGER  aspergillus niger  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6507 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ASPERGILLUS NIGER VAR. NIGER (ASPERGILLUS NIGER VAR. NIGER) ASPERGILLUS NIGER VAR. NIGER 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6507-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

AUREOBASIDIUM PULLULANS VAR PULLULANS  pullularia pullulans  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6509 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AUREOBASIDIUM PULLULANS VAR. PULLUTANS (AUREOBASIDIUM PULLULANS VAR. PULLUTANS) AUREOBASIDIUM PULLULANS VAR. PULLUTANS 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6509-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

BOTRYTIS CINEREA  botrytis cinerea  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6512 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BOTRYTIS CINEREA (BOTRYTIS CINEREA) BOTRYTIS CINEREA 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6512-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CANDIDA ALBICANS  candida albicans  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6514 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CANDIDA ALBICANS (CANDIDA ALBICANS) CANDIDA ALBICANS 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6514-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CHAETOMIUM GLOBOSUM  chaetomium globosum  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6516 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHAETOMIUM GLOBOSUM (CHAETOMIUM GLOBOSUM) CHAETOMIUM GLOBOSUM 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6516-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CLADOSPORIUM CLADOSPORIOIDES  cladosporium cladosporioides hormodendrum clad  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6518 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CLADOSPORIUM CLADOSPORIOIDES (CLADOSPORIUM CLADOSPORIOIDES) CLADOSPORIUM CLADOSPORIOIDES 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6518-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CLADOSPORIUM SPHAEROSPERMUM  cladosporium sphaerospermum hormodendrum hordei  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6520 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CLADOSPORIUM SPHAEROSPERMUM (CLADOSPORIUM SPHAEROSPERMUM) CLADOSPORIUM SPHAEROSPERMUM 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6520-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

COCHLIOBOLUS SATIVUS  helminthosporium sorokinianum  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6524 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength COCHLIOBOLUS SATIVUS (COCHLIOBOLUS SATIVUS) COCHLIOBOLUS SATIVUS 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6524-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

EPICOCCUM NIGRUM  epicoccum nigrum  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6526 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength EPICOCCUM NIGRUM (EPICOCCUM NIGRUM) EPICOCCUM NIGRUM 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6526-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

FUSARIUM OXYSPORUM VASINFECTUM  fusarium spp  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6529 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength FUSARIUM OXYSPORUM VASINFECTUM (FUSARIUM OXYSPORUM VASINFECTUM) FUSARIUM OXYSPORUM VASINFECTUM 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6529-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

HELMINTHOSPORIUM SOLANI  helminthosporium solani spondylocladium  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6533 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HELMINTHOSPORIUM SOLANI (HELMINTHOSPORIUM SOLANI) HELMINTHOSPORIUM SOLANI 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6533-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

MUCOR PLUMBEUS  mucor spp  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6536 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MUCOR PLUMBEUS (MUCOR PLUMBEUS) MUCOR PLUMBEUS 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6536-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

NEUROSPORA INTERMEDIA  neurospora spp  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6538 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NEUROSPORA INTERMEDIA (NEUROSPORA INTERMEDIA) NEUROSPORA INTERMEDIA 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6538-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

KHUSKIA ORYZAE  nigrospora spp  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6540 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength KHUSKIA ORYZAE (KHUSKIA ORYZAE) KHUSKIA ORYZAE 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6540-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PHOMA EXIGUA VAR EXIGUA  phoma herbarum  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6543 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PHOMA EXIGUA VAR. EXIGUA (PHOMA EXIGUA VAR. EXIGUA) PHOMA EXIGUA VAR. EXIGUA 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6543-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

RHIZOPUS ARRHIZUS VAR ARRHIZUS  rhizopus spp  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6545 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RHIZOPUS ARRHIZUS VAR. ARRHIZUS (RHIZOPUS ARRHIZUS VAR. ARRHIZUS) RHIZOPUS ARRHIZUS VAR. ARRHIZUS 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6545-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

RHODOTORULA RUBRA  rhodotorula rubra  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6548 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RHODOTORULA RUBRA (RHODOTORULA RUBRA) RHODOTORULA RUBRA 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6548-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

USTILAGO MAYDIS  corn smut  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6550 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength USTILAGO MAYDIS (USTILAGO MAYDIS) USTILAGO MAYDIS 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6550-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

USTILAGO TRITICI  wheat smut  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6552 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength USTILAGO TRITICI (USTILAGO TRITICI) USTILAGO TRITICI 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6552-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

STEMPHYLIUM SOLANI  stemphylium spp  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6553 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength STEMPHYLIUM SOLANI (STEMPHYLIUM SOLANI) STEMPHYLIUM SOLANI 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6553-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

TRICHOPHYTON MENTAGROPHYTES  trichophyton mentagrophytes  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6556 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TRICHOPHYTON MENTAGROPHYTES (TRICHOPHYTON MENTAGROPHYTES) TRICHOPHYTON MENTAGROPHYTES 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6556-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PENICILLIUM CHRYSOGENUM VAR CHRYSOGENUM  yeast saccharomyces cerevisiae  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6558 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM 0.10 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6558-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ACACIA  acacia  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6600 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACACIA (ACACIA) ACACIA 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6600-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ALNUS INCANA SSP RUGOSA POLLEN  white alder  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6601 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALNUS INCANA SUBSP. RUGOSA POLLEN (ALNUS INCANA SUBSP. RUGOSA POLLEN) ALNUS INCANA SUBSP. RUGOSA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6601-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

MEDICAGO SATIVA POLLEN  alfalfa  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6602 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MEDICAGO SATIVA POLLEN (MEDICAGO SATIVA POLLEN) MEDICAGO SATIVA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6602-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

FRAXINUS AMERICANA POLLEN  white ash  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6603 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength FRAXINUS AMERICANA POLLEN (FRAXINUS AMERICANA POLLEN) FRAXINUS AMERICANA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6603-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PASPALUM NOTATUM POLLEN  bahia grass  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6605 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PASPALUM NOTATUM POLLEN (PASPALUM NOTATUM POLLEN) PASPALUM NOTATUM POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6605-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

MORELLA CERIFERA POLLEN  bayberry wax myrtle  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6606 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MORELLA CERIFERA POLLEN (MORELLA CERIFERA POLLEN) MORELLA CERIFERA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6606-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

FAGUS GRANDIFOLIA POLLEN  beech  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6607 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength FAGUS GRANDIFOLIA POLLEN (FAGUS GRANDIFOLIA POLLEN) FAGUS GRANDIFOLIA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6607-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

BETULA LENTA POLLEN  black birch  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6608 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BETULA LENTA POLLEN (BETULA LENTA POLLEN) BETULA LENTA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6608-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

BETULA NIGRA POLLEN  river birch red  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6609 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BETULA NIGRA POLLEN (BETULA NIGRA POLLEN) BETULA NIGRA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6609-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

BETULA LENTA POLLEN  white birch  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6610 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BETULA LENTA POLLEN (BETULA LENTA POLLEN) BETULA LENTA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6610-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ACER NEGUNDO POLLEN  box elder ash leaf maple  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6612 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACER NEGUNDO POLLEN (ACER NEGUNDO POLLEN) ACER NEGUNDO POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6612-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

AMARANTHUS PALMERI POLLEN  carelessweed  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6613 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMARANTHUS PALMERI POLLEN (AMARANTHUS PALMERI POLLEN) AMARANTHUS PALMERI POLLEN 0.025 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6613-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

JUNIPERUS ASHEI POLLEN  mountain cedar  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6614 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength JUNIPERUS ASHEI POLLEN (JUNIPERUS ASHEI POLLEN) JUNIPERUS ASHEI POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6614-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

JUNIPERUS VIRGINIANA POLLEN  red cedar  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6615 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength JUNIPERUS VIRGINIANA POLLEN (JUNIPERUS VIRGINIANA POLLEN) JUNIPERUS VIRGINIANA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6615-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

XANTHIUM STRUMARIUM VAR CANADENSE POLLEN  cocklebur  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6616 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength XANTHIUM STRUMARIUM VAR. CANADENSE POLLEN (XANTHIUM STRUMARIUM VAR. CANADENSE POLLEN) XANTHIUM STRUMARIUM VAR. CANADENSE POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6616-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

POPULUS DELTOIDES POLLEN  eastern cottonwood common  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6618 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POPULUS DELTOIDES POLLEN (POPULUS DELTOIDES POLLEN) POPULUS DELTOIDES POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6618-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CUPRESSUS ARIZONICA POLLEN  arizona cypress  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6619 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CUPRESSUS ARIZONICA POLLEN (CUPRESSUS ARIZONICA POLLEN) CUPRESSUS ARIZONICA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6619-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

TAXODIUM DISTICHUM POLLEN  bald cypress  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6620 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TAXODIUM DISTICHUM POLLEN (TAXODIUM DISTICHUM POLLEN) TAXODIUM DISTICHUM POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6620-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

RUMEX ACETOSELLA POLLEN  sour dock sheep sorrel  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6621 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RUMEX ACETOSELLA POLLEN (RUMEX ACETOSELLA POLLEN) RUMEX ACETOSELLA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6621-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

RUMEX CRISPUS POLLEN  yellow dock  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6622 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RUMEX CRISPUS POLLEN (RUMEX CRISPUS POLLEN) RUMEX CRISPUS POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6622-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ULMUS AMERICANA POLLEN  american elm  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6623 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ULMUS AMERICANA POLLEN (ULMUS AMERICANA POLLEN) ULMUS AMERICANA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6623-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

SOLIDAGO CANADENSIS POLLEN  goldenrod  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6625 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SOLIDAGO CANADENSIS POLLEN (SOLIDAGO CANADENSIS POLLEN) SOLIDAGO CANADENSIS POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6625-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CELTIS OCCIDENTALIS POLLEN  hackberry  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6626 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CELTIS OCCIDENTALIS POLLEN (CELTIS OCCIDENTALIS POLLEN) CELTIS OCCIDENTALIS POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6626-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CARYA OVATA POLLEN  shagbark hickory  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6627 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CARYA OVATA POLLEN (CARYA OVATA POLLEN) CARYA OVATA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6627-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

SORGHUM HALEPENSE POLLEN  johnson grass  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6629 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SORGHUM HALEPENSE POLLEN (SORGHUM HALEPENSE POLLEN) SORGHUM HALEPENSE POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6629-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

JUNIPERUS CALIFORNICA POLLEN  western juniper  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6630 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength JUNIPERUS CALIFORNICA POLLEN (JUNIPERUS CALIFORNICA POLLEN) JUNIPERUS CALIFORNICA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6630-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

KOCHIA SCOPARIA POLLEN  kochia firebush  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6631 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength KOCHIA SCOPARIA POLLEN (KOCHIA SCOPARIA POLLEN) KOCHIA SCOPARIA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6631-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CHENOPODIUM ALBUM POLLEN  lambs quarters  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6632 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHENOPODIUM ALBUM POLLEN (CHENOPODIUM ALBUM POLLEN) CHENOPODIUM ALBUM POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6632-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ACER RUBRUM POLLEN  red maple  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6634 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACER RUBRUM POLLEN (ACER RUBRUM POLLEN) ACER RUBRUM POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6634-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ACER SACCHARUM POLLEN  sugar maple  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6635 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACER SACCHARUM POLLEN (ACER SACCHARUM POLLEN) ACER SACCHARUM POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6635-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

IVA XANTHIFOLIA POLLEN  burweed marshelder  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6636 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength IVA XANTHIFOLIA POLLEN (IVA XANTHIFOLIA POLLEN) IVA XANTHIFOLIA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6636-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

IVA ANNUA VAR ANNUA POLLEN  rough marshelder  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6637 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength IVA ANNUA VAR. ANNUA POLLEN (IVA ANNUA VAR. ANNUA POLLEN) IVA ANNUA VAR. ANNUA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6637-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PROSOPIS JULIFLORA POLLEN  mesquite  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6638 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PROSOPIS JULIFLORA POLLEN (PROSOPIS JULIFLORA POLLEN) PROSOPIS JULIFLORA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6638-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ARTEMISIA VULGARIS POLLEN  common mugwort  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6639 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ARTEMISIA VULGARIS POLLEN (ARTEMISIA VULGARIS POLLEN) ARTEMISIA VULGARIS POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6639-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

MORUS RUBRA POLLEN  red mulberry  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6640 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MORUS RUBRA POLLEN (MORUS RUBRA POLLEN) MORUS RUBRA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6640-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

MORUS ALBA POLLEN  white mulberry  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6641 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MORUS ALBA POLLEN (MORUS ALBA POLLEN) MORUS ALBA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6641-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

QUERCUS RUBRA POLLEN  red oak  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6642 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength QUERCUS RUBRA POLLEN (QUERCUS RUBRA POLLEN) QUERCUS RUBRA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6642-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

QUERCUS VIRGINIANA POLLEN  virginia live oak  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6643 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength QUERCUS VIRGINIANA POLLEN (QUERCUS VIRGINIANA POLLEN) QUERCUS VIRGINIANA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6643-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

QUERCUS ALBA POLLEN  white oak  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6644 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength QUERCUS ALBA POLLEN (QUERCUS ALBA POLLEN) QUERCUS ALBA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6644-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

OLEA EUROPAEA POLLEN  olive pollen  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6646 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OLEA EUROPAEA POLLEN (OLEA EUROPAEA POLLEN) OLEA EUROPAEA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6646-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

SYAGRUS ROMANZOFFIANA POLLEN  queen palm coco palm  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6647 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SYAGRUS ROMANZOFFIANA POLLEN (SYAGRUS ROMANZOFFIANA POLLEN) SYAGRUS ROMANZOFFIANA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6647-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CARYA ILLINOINENSIS POLLEN  pecan pollen  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6648 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CARYA ILLINOINENSIS POLLEN (CARYA ILLINOINENSIS POLLEN) CARYA ILLINOINENSIS POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6648-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

AMARANTHUS RETROFLEXUS POLLEN  rough pigweed  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6649 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMARANTHUS RETROFLEXUS POLLEN (AMARANTHUS RETROFLEXUS POLLEN) AMARANTHUS RETROFLEXUS POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6649-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PINUS STROBUS POLLEN  white pine  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6651 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PINUS STROBUS POLLEN (PINUS STROBUS POLLEN) PINUS STROBUS POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6651-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PLANTAGO LANCEOLATA POLLEN  english plantain  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6652 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PLANTAGO LANCEOLATA POLLEN (PLANTAGO LANCEOLATA POLLEN) PLANTAGO LANCEOLATA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6652-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

POPULUS ALBA POLLEN  white poplar  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6654 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POPULUS ALBA POLLEN (POPULUS ALBA POLLEN) POPULUS ALBA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6654-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

LIGUSTRUM VULGARE POLLEN  privet  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6656 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIGUSTRUM VULGARE POLLEN (LIGUSTRUM VULGARE POLLEN) LIGUSTRUM VULGARE POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6656-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ELYMUS REPENS POLLEN  quack grass  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6657 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ELYMUS REPENS POLLEN (ELYMUS REPENS POLLEN) ELYMUS REPENS POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6657-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

AMBROSIA TRIFIDA POLLEN  tall ragweed giant  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6658 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMBROSIA TRIFIDA POLLEN (AMBROSIA TRIFIDA POLLEN) AMBROSIA TRIFIDA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6658-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

SALSOLA KALI POLLEN  russian thistle  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6659 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALSOLA KALI POLLEN (SALSOLA KALI POLLEN) SALSOLA KALI POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6659-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ARTEMISIA TRIDENTATA POLLEN  common sagebrush  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6670 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ARTEMISIA TRIDENTATA POLLEN (ARTEMISIA TRIDENTATA POLLEN) ARTEMISIA TRIDENTATA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6670-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

LIQUIDAMBAR STYRACIFLUA POLLEN  sweetgum  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6671 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIQUIDAMBAR STYRACIFLUA POLLEN (LIQUIDAMBAR STYRACIFLUA POLLEN) LIQUIDAMBAR STYRACIFLUA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6671-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PLATANUS OCCIDENTALIS POLLEN  american sycamore  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6672 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PLATANUS OCCIDENTALIS POLLEN (PLATANUS OCCIDENTALIS POLLEN) PLATANUS OCCIDENTALIS POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6672-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

JUGLANS NIGRA POLLEN  black pollen walnut  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6674 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength JUGLANS NIGRA POLLEN (JUGLANS NIGRA POLLEN) JUGLANS NIGRA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6674-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

AILANTHUS ALTISSIMA POLLEN  ailanthus tree of heaven  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6677 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AILANTHUS ALTISSIMA POLLEN (AILANTHUS ALTISSIMA POLLEN) AILANTHUS ALTISSIMA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6677-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

POPULUS TREMULOIDES POLLEN  aspen  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6681 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POPULUS TREMULOIDES POLLEN (POPULUS TREMULOIDES POLLEN) POPULUS TREMULOIDES POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6681-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

POA ANNUA POLLEN  annual bluegrass  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6689 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POA ANNUA POLLEN (POA ANNUA POLLEN) POA ANNUA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6689-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

BROMUS INERMIS POLLEN  brome grass  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6691 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BROMUS INERMIS POLLEN (BROMUS INERMIS POLLEN) BROMUS INERMIS POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6691-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ZEA MAYS POLLEN  corn pollen  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6697 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZEA MAYS POLLEN (ZEA MAYS POLLEN) ZEA MAYS POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6697-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

POPULUS FREMONTII POLLEN  fremont cottonwood  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6700 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POPULUS FREMONTII POLLEN (POPULUS FREMONTII POLLEN) POPULUS FREMONTII POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6700-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

POPULUS DELTOIDES SSP MONILIFERA POLLEN  western cottonwood  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6701 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POPULUS DELTOIDES SUBSP. MONILIFERA POLLEN (POPULUS DELTOIDES SUBSP. MONILIFERA POLLEN) POPULUS DELTOIDES SUBSP. MONILIFERA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6701-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

EUPATORIUM CAPILLIFOLIUM POLLEN  dog fennel  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6706 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength EUPATORIUM CAPILLIFOLIUM POLLEN (EUPATORIUM CAPILLIFOLIUM POLLEN) EUPATORIUM CAPILLIFOLIUM POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6706-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ULMUS CRASSIFOLIA POLLEN  cedar elm  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6709 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ULMUS CRASSIFOLIA POLLEN (ULMUS CRASSIFOLIA POLLEN) ULMUS CRASSIFOLIA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6709-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ULMUS PUMILA POLLEN  chinese elm  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6710 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ULMUS PUMILA POLLEN (ULMUS PUMILA POLLEN) ULMUS PUMILA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6710-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

EUCALYPTUS GLOBULUS POLLEN  eucalyptus  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6712 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength EUCALYPTUS GLOBULUS POLLEN (EUCALYPTUS GLOBULUS POLLEN) EUCALYPTUS GLOBULUS POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6712-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CORYLUS AMERICANA POLLEN  hazelnut pollen  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6714 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CORYLUS AMERICANA POLLEN (CORYLUS AMERICANA POLLEN) CORYLUS AMERICANA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6714-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ROBINIA PSEUDOACACIA POLLEN  black locust  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6722 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ROBINIA PSEUDOACACIA POLLEN (ROBINIA PSEUDOACACIA POLLEN) ROBINIA PSEUDOACACIA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6722-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

MELALEUCA QUINQUENERVIA POLLEN  melaleuca pollen  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6728 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MELALEUCA QUINQUENERVIA POLLEN (MELALEUCA QUINQUENERVIA POLLEN) MELALEUCA QUINQUENERVIA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6728-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CHENOPODIUM AMBROSIOIDES POLLEN  mexican tea  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6731 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHENOPODIUM AMBROSIOIDES POLLEN (CHENOPODIUM AMBROSIOIDES POLLEN) CHENOPODIUM AMBROSIOIDES POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6731-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

QUERCUS AGRIFOLIA POLLEN  california live oak coast  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6736 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength QUERCUS AGRIFOLIA POLLEN (QUERCUS AGRIFOLIA POLLEN) QUERCUS AGRIFOLIA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6736-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

QUERCUS ALBA POLLEN  wild pollen oat  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6741 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength QUERCUS ALBA POLLEN (QUERCUS ALBA POLLEN) QUERCUS ALBA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6741-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

SCHINUS MOLLE POLLEN  california pepper tree  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6743 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SCHINUS MOLLE POLLEN (SCHINUS MOLLE POLLEN) SCHINUS MOLLE POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6743-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

AMARANTHUS SPINOSUS POLLEN  spiny pigweed  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6744 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMARANTHUS SPINOSUS POLLEN (AMARANTHUS SPINOSUS POLLEN) AMARANTHUS SPINOSUS POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6744-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CASUARINA EQUISETIFOLIA POLLEN  australian pine beefwood  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6745 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CASUARINA EQUISETIFOLIA POLLEN (CASUARINA EQUISETIFOLIA POLLEN) CASUARINA EQUISETIFOLIA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6745-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PINUS ECHINATA POLLEN  yellow pine  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6748 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PINUS ECHINATA POLLEN (PINUS ECHINATA POLLEN) PINUS ECHINATA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6748-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

AMBROSIA ACANTHICARPA POLLEN  false ragweed bur  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6749 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMBROSIA ACANTHICARPA POLLEN (AMBROSIA ACANTHICARPA POLLEN) AMBROSIA ACANTHICARPA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6749-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

AMBROSIA TENUIFOLIA POLLEN  slender ragweed  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6750 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMBROSIA TENUIFOLIA POLLEN (AMBROSIA TENUIFOLIA POLLEN) AMBROSIA TENUIFOLIA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6750-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

AMBROSIA BIDENTATA POLLEN  southern ragweed  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6751 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMBROSIA BIDENTATA POLLEN (AMBROSIA BIDENTATA POLLEN) AMBROSIA BIDENTATA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6751-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

AMBROSIA PSILOSTACHYA POLLEN  western ragweed  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6752 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMBROSIA PSILOSTACHYA POLLEN (AMBROSIA PSILOSTACHYA POLLEN) AMBROSIA PSILOSTACHYA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6752-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

LOLIUM PERENNE SSP MULTIFLORUM POLLEN  italian rye grass  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6754 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LOLIUM PERENNE SSP. MULTIFLORUM POLLEN (LOLIUM PERENNE SSP. MULTIFLORUM POLLEN) LOLIUM PERENNE SSP. MULTIFLORUM POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6754-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ARTEMISIA FRIGIDA POLLEN  prairie sage  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6755 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ARTEMISIA FRIGIDA POLLEN (ARTEMISIA FRIGIDA POLLEN) ARTEMISIA FRIGIDA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6755-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

DISTICHLIS SPICATA POLLEN  salt grass  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6757 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DISTICHLIS SPICATA POLLEN (DISTICHLIS SPICATA POLLEN) DISTICHLIS SPICATA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6757-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

HOLCUS LANATUS POLLEN  velvet grass  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6760 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOLCUS LANATUS POLLEN (HOLCUS LANATUS POLLEN) HOLCUS LANATUS POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6760-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

JUGLANS NIGRA POLLEN  california walnut black pollen  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6761 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength JUGLANS NIGRA POLLEN (JUGLANS NIGRA POLLEN) JUGLANS NIGRA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6761-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

JUGLANS REGIA POLLEN  english walnut pollen  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6762 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength JUGLANS REGIA POLLEN (JUGLANS REGIA POLLEN) JUGLANS REGIA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6762-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

TRITICUM AESTIVUM POLLEN  wheat pollen  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6763 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TRITICUM AESTIVUM POLLEN (TRITICUM AESTIVUM POLLEN) TRITICUM AESTIVUM POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6763-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

ARTEMISIA ANNUA POLLEN  common wormwood annual  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6764 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ARTEMISIA ANNUA POLLEN (ARTEMISIA ANNUA POLLEN) ARTEMISIA ANNUA POLLEN 0.05 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6764-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

AMARANTHUS TUBERCULATUS POLLEN  water hemp  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6771 Route of Administration PERCUTANEOUS DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMARANTHUS TUBERCULATUS POLLEN (AMARANTHUS TUBERCULATUS POLLEN) AMARANTHUS TUBERCULATUS POLLEN 0.025 g  in 1 mL

Inactive Ingredients Ingredient Name Strength GLYCERIN 0.5 mL  in 1 mL PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6771-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

HOUSE DUST  house dust  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6001 Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOUSE DUST (HOUSE DUST) HOUSE DUST 1000 [PNU]  in 1 mL

Inactive Ingredients Ingredient Name Strength PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6001-05 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

BOS TAURUS SKIN  cattle epithelium  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6301 Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BOS TAURUS SKIN (BOS TAURUS SKIN) BOS TAURUS SKIN 1000 [PNU]  in 1 mL

Inactive Ingredients Ingredient Name Strength PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6301-05 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

COTTON FIBER  cotton linters  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6303 Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength COTTON FIBER (COTTON FIBER) COTTON FIBER 0.001 g  in 1 mL

Inactive Ingredients Ingredient Name Strength PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6303-05 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CANIS LUPUS FAMILIARIS SKIN  dog epithelium  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6305 Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CANIS LUPUS FAMILIARIS SKIN (CANIS LUPUS FAMILIARIS SKIN) CANIS LUPUS FAMILIARIS SKIN 1000 [PNU]  in 1 mL

Inactive Ingredients Ingredient Name Strength PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6305-05 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

CAVIA PORCELLUS SKIN  guinea pig epithelium  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6308 Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CAVIA PORCELLUS SKIN (CAVIA PORCELLUS SKIN) CAVIA PORCELLUS SKIN 1000 [PNU]  in 1 mL

Inactive Ingredients Ingredient Name Strength PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6308-05 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

EQUUS CABALLUS SKIN  horse epithelium  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6310 Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength EQUUS CABALLUS SKIN (EQUUS CABALLUS SKIN) EQUUS CABALLUS SKIN 1000 [PNU]  in 1 mL

Inactive Ingredients Ingredient Name Strength PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6310-05 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

MUS MUSCULUS SKIN  mouse epithelium  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6316 Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MUS MUSCULUS SKIN (MUS MUSCULUS SKIN) MUS MUSCULUS SKIN 1000 [PNU]  in 1 mL

Inactive Ingredients Ingredient Name Strength PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6316-05 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

RABBIT  rabbit epithelium  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6319 Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RABBIT (RABBIT) RABBIT 1000 [PNU]  in 1 mL

Inactive Ingredients Ingredient Name Strength PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6319-05 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

SOLENOPSIS INVICTA  fire ant  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6401 Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SOLENOPSIS INVICTA (SOLENOPSIS INVICTA) SOLENOPSIS INVICTA 10 [PNU]  in 1 mL

Inactive Ingredients Ingredient Name Strength PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6401-05 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

PERIPLANETA AMERICANA  american cockroach  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6402 Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PERIPLANETA AMERICANA (PERIPLANETA AMERICANA) PERIPLANETA AMERICANA 100 [PNU]  in 1 mL

Inactive Ingredients Ingredient Name Strength PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6402-05 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
BLA	BLA103753	01/01/1965

BLATELLA GERMANICA  german cockroach  injection, solution

Product Information Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6407 Route of Administration INTRADERMAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BLATELLA GERMANICA (BLATELLA GERMANICA) BLATELLA GERMANICA 100 [PNU]  in 1 mL

Inactive Ingredients Ingredient Name Strength PHENOL 0.004 mL  in 1 mL SODIUM CHLORIDE 0.009 g  in 1 mL SODIUM BICARBONATE 0.00275 g  in 1 mL HYDROCHLORIC ACID   SODIUM HYDROXIDE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0268-6407-05 5 mL In 1 VIAL, MULTI-DOSE None