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Ana-Lex Cream

Generic Name: hydrocortisone acetate and lidocaine hydrochloride
Dosage Form: cream

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Ana-Lex™
Rx Only

DESCRIPTION: Each gram of Ana-Lex™ contains the active ingredients hydrocortisone acetate 20 mg and lidocaine hydrochloride 20 mg. Also contains a 1% (10 mg per gram) Coleus Forskohlii Base.* The inactive ingredients include aluminum sulfate, calcium acetate, carbomer, cetyl alcohol, citric acid, glycerine, methyl paraben, mineral oil, polycarophil, propyl paraben, propylene glycol, purified water, sodium citrate, sodium hydroxide, sodium lauryl sulfate, sorbitan stearate, stearic acid, stearyl alcohol, trolamine, urea and white petrolatum.

Hydrocortisone acetate has a chemical name pregn-4-ene-3, 20-dione, 21-(acetyloxy)-11,17-dihydroxy-(11ß)-. It has the following structural formula:

Lidocaine HCl is chemically designated as acetamide, 2(diethylamino)- N-(2,6-dimethylphenyl), and has the following structure:

CLINICAL PHARMACOLOGY:

MECHANISM OF ACTION: Ana-Lex™ releases lidocaine and hydrocortisone from a coleus base to increase the antimicrobial function by inhibiting microbial growth, thereby enhancing the function of the product. Hydrocortisone acetate provides relief of inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses.

PHARMACOKINETICS: Lidocaine may be absorbed following topical administration to mucous membranes, its rate and extent of absorption depending upon the specific site of application, duration of exposure, concentration, and total dosage. In general, the rate of absorption of local anesthetic agents following topical application occurs most rapidly after intratracheal administration. Lidocaine is also well-absorbed from the gastrointestinal tract, but little intact drug appears in the circulation because of biotransformation in the liver.

Lidocaine HCl is metabolized rapidly by the liver, and metabolites and unchanged drug are excreted by the kidneys. Biotransformation includes oxidative N-dealkylation, ring hydroxylation, cleavage of the amide linkage, and conjugation. N-dealkylation, a major pathway of biotransformation, yields the metabolites monoethylglycinexylidide and glycinexylidide. The pharmacological/toxicological actions of these metabolites are similar to, but less potent than, those of lidocaine. Approximately 90% of lidocaine administered is excreted in the form of various metabolites, and less than 10% is excreted unchanged. The primary metabolite in urine is a conjugate of 4-hydroxy-2, 6-dimethylaniline.

The plasma binding of lidocaine is dependent on drug concentration, and the fraction bound decreases with increasing concentration. At concentrations of 1 to 4 g of free base per mL, 60 to 80 percent of lidocaine is protein bound. Binding is also dependent on the plasma concentration of the alpha-1-acid glycoprotein.

Lidocaine crosses the blood-brain and placental barriers, presumably by passive diffusion.

Studies of lidocaine metabolism following intravenous bolus injections have shown that the elimination half-life of this agent is typically 1.5 to 2 hours. Because of the rapid rate at which lidocaine is metabolized, any condition that affects liver function may alter lidocaine kinetics. The half-life may be prolonged two-fold or more in patients with liver dysfunction. Renal dysfunction does not affect lidocaine kinetics but may increase the accumulation of metabolites.

Factors such as acidosis and the use of CNS stimulants and depressants affect the CNS levels of lidocaine required to produce overt systemic effects. Objective adverse manifestations become increasingly apparent with increasing venous plasma levels above 6 g free base per mL. In the rhesus monkey, arterial blood levels of 18-21 g/mL have been shown to be threshold for convulsive activity.

The extent of percutaneous absorption of topical corticosteroids is determined by many factors including the Base, the integrity of the epidermal barrier, and the use of occlusive dressings. Topical corticosteroids can be absorbed from normal intact skin. Inflammation and/or other disease processes in the skin increase percutaneous absorption. Occlusive dressings substantially increase the percutaneous absorption of topical corticosteroids. Thus, occlusive dressings may be a valuable therapeutic adjunct for treatment of resistant dermatoses.

Once absorbed through the skin, topical corticosteroids are handled through pharmacokinetic pathways similar to systemically administered corticosteroids. Corticosteroids are bound to plasma protein in varying degrees. Corticosteroids are metabolized primarily in the liver and are then excreted by the kidneys. Some of the topical corticosteroids and their metabolites are also excreted into the bile.

INDICATIONS: Ana-Lex™ is used for the anti-inflammatory and anesthetic relief of itching, pain, soreness and discomfort due to hemorrhoids, anal fissures, pruritus ani and similar conditions of the anal area.

CONTRAINDICATIONS: Ana-Lex™ should not be used in patients with a history of sensitivity to any of its ingredients or adverse reactions to lidocaine or amide anesthetics, which usually do not cross-react with “caine” ester type anesthetics. If excessive irritation and significant worsening occur, discontinue use and seek the advice of your physician. Ana-Lex™ should be used cautiously in those with impaired liver function, as well as the very ill or very elderly and those with significant liver disease. Ana-Lex™ should be used with caution in patients receiving antiarrhythmic drugs of Class I since the adverse effects are additive and generally synergistic. Ana-Lex™ is contraindicated for tuberculous or fungal lesions or skin vaccinia, varicella and acute herpes simplex. Topical corticosteroids are contraindicated in those patients with a history of hypersensitivity to any of the components of the preparation.

WARNINGS: For external use only. Not for ophthalmic use. Product could harm small children if chewed or swallowed.

KEEP PRODUCT AND CLEANSING WIPES OUT OF THE REACH OF CHILDREN.

Topical formulations of lidocaine may be absorbed to a greater extent through mucous membranes and abraded, fissured or irritated skin than through intact skin. Ana-Lex™ should not be ingested or applied into the mouth, inside of the nose or in the eyes. Ana-Lex™ should not be used in the ears. Any situation where lidocaine penetrates beyond the tympanic membrane into the middle ear is contraindicated because of ototoxicity associated with lidocaine observed in animals when instilled in the middle ear. Ana-Lex™ should not come into contact with the eye or be applied into the eye because of the risk of severe eye irritation and the loss of eye surface sensation which reduces protective reflexes and can lead to corneal irritation and possibly abrasion. If eye contact occurs, rinse out the eye immediately with saline or water and protect the eye surface until sensation is restored.

PRECAUTIONS: If irritation or sensitivity occurs or infection appears, discontinue use and institute appropriate therapy. If extensive areas are treated, the possibility of systemic absorption exists. Systemic absorption of topical steroids has produced reversible hypothalamic-pituitary-adrenal (HPA) axis suppression, manifestations of Cushing’s syndrome, hyperglycemia, and glycosuria in some patients. Conditions which augment systemic absorption include the application of the more potent steroids, use over large surface areas, prolonged use, and the addition of occlusive dressings. Therefore, patients receiving a large dose of potent topical steroids applied to a large surface area or under an occlusive dressing should be evaluated periodically for evidence of HPA axis suppression. If noted, an attempt should be made to withdraw the drug, to reduce the frequency of application, or to substitute a less potent steroid. Recovery of the HPA axis function is generally complete upon discontinuation of the drug. Infrequently, signs and symptoms of steroid withdrawal may occur, requiring supplemental systemic corticosteroids. Children may absorb proportionately larger amounts of topical corticosteroids and thus be more susceptible to systemic toxicity. If irritation develops, topical steroids should be discontinued and appropriate therapy instituted. In the presence of dermatological infections, the use of an appropriate antifungal or antibacterial agent should be started. If a favorable response does not occur promptly, the corticosteroid should be discontinued until the infection has been adequately controlled.

Carcinogenesis, Mutagenesis, and Impairment of Fertility: Long-term animal studies have not been conducted to evaluate the carcinogenic potential or the effect on fertility of topical corticosteroids.

Studies to determine mutagenicity with prednisolone and hydrocortisone have revealed negative results.

Studies of lidocaine in animals to evaluate the carcinogenic and mutagenic potential of the effect on fertility have not been performed.

Use in Pregnancy: Teratogenic Effects: Pregnancy Category C. Reproduction studies have been performed for lidocaine in rats at doses up to 6.6 times the human dose and have revealed no evidence of harm to the fetus caused by lidocaine. There are however, no adequate and well-controlled studies in pregnant women. Animal reproduction studies are not always predictive of human response. General consideration should be given to this fact before administering lidocaine to women of childbearing potential, especially during early pregnancy when maximum organogenesis takes place.

Corticosteroids are generally teratogenic in laboratory animals when administered systemically at relatively low dosage levels. The more potent corticosteroids have been shown to be teratogenic after dermal application in laboratory animals. There are no adequate and well-controlled studies in pregnant women on teratogenic effects from topically applied corticosteroids. Therefore, topical corticosteroids should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus. Drugs of this class should not be used extensively on pregnant patients, in large amounts or for prolonged periods of time.

Nursing Mothers: It is not known whether this drug is excreted in human milk. Caution should be exercised when this drug is administered to a nursing mother because many drugs are excreted in human milk.

Pediatric Use: Safety and efficacy in children have not been established.

ADVERSE REACTIONS: During or immediately following application of Ana-Lex™ there may be transient stinging or burning from open areas of skin, or transient blanching (lightening) or erythema (redness) of the skin.

DOSAGE AND ADMINISTRATION: Remove the cleansing wipe from package and gently clean the affected area. Discard wipe after use. Please note that the cleansing wipe does not contain any active ingredients. Remove the child resistant cap and foil seal from the tube of Ana-Lex HC and screw on the provided applicator. Gently squeeze the tube until the applicator is full and a small amount of the cream comes out of the applicator opening. Insert the applicator tip gently into the anus and continue squeezing the body of the tube as it is moved around the areas of discomfort until the tube is empty. Do not completely insert the tube into the anus or insert deep into the rectum. Once the application is completed, the tube and applicator should be removed and discarded. Note that an adequate amount of Ana-Lex™ for an application to the anal and peri-anal area will be applied through the applicator tip by gently squeezing the tube during application. Ana-Lex™ should not be used in excess of recommendations or for prolonged use in the anal canal. If the condition does not respond to repeated courses of Ana-Lex™ or should worsen, discontinue use and seek the advice of your physician.

HOW SUPPLIED: Ana-Lex™ is supplied commercially as a KIT (NDC 75854-102-24) and non-commercially as a Physician Sample Kit (75854-102-01):

  • Ana-Lex™ KIT (NDC 75854-102-24) contains 24 Single-Use Tubes (4g), Applicators and Cleansing Wipes.
  • Ana-Lex™ Physician Sample Kit (NDC 75854-102-01) contains 1 Single-Use Tube (4g) (NDC 75854-102-04), Applicator and Cleansing Wipe.

KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN.

Store at Controlled Room Temperature 20°C to 25°C (68°F to 77°F) excursions permitted between 15°C and 30°C (between 59°F and 86°F). Brief exposure to temperatures up to 40°C (104°F) may be tolerated provided the mean kinetic temperature does not exceed 25°C (77°F); however, such exposure should be minimized.

* Coleus Forskohlii Base (coleus oil) is comprised of:
a-Pinene CAS# 80-56-8
b-Pinene CAS# 127-91-3 Bornyl Acetate CAS# 5655-61-8
Decanal CAS# 112-31-2
Protected by one or more claims of Patent 6,607,712
Under license from Sabinsa Corporation.

Manufactured for:
Avion Pharmaceuticals, LLC
Alpharetta, GA 30022
888.61.AVION

Rev 0614

PRINCIPAL DISPLAY PANEL - 4 gram carton label

RX ONLY      Net wt 4 g       NDC 75854-102-04

ANA-LEX™

Hydrocortisone Acetate 2% Lidocaine HCl 2%
in a 1% Coleus Forskohlii Base

FOR EXTERNAL USE ONLY. NOT FOR OPHTHALMIC USE.

Directions Use only as directed by a physician. See package insert for
complete directions.

Store at Controlled Room Temperature 20°C to 25°C (68°F to 77°F)
excursions permitted between 15°C and 30°C (between 59°F and 86°F).

KEEP OUT OF THE REACH OF CHILDREN.

AVION
PHARMACEUTICALS

Manufactured for
Avion Pharmaceuticals, LLC
Alpharetta, GA 30022
Rev 0614

ANA-LEX 
hydrocortisone acetate and lidocaine hydrochloride cream
Product Information
Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:75854-102
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
HYDROCORTISONE ACETATE (HYDROCORTISONE) HYDROCORTISONE ACETATE 20 mg  in 1 g
LIDOCAINE HYDROCHLORIDE (LIDOCAINE) LIDOCAINE HYDROCHLORIDE ANHYDROUS 20 mg  in 1 g
Inactive Ingredients
Ingredient Name Strength
PLECTRANTHUS BARBATUS WHOLE 10 mg  in 1 g
ALUMINUM SULFATE  
CALCIUM ACETATE  
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED)  
CETYL ALCOHOL  
CITRIC ACID MONOHYDRATE  
GLYCERIN  
METHYLPARABEN  
MINERAL OIL  
POLYCARBOPHIL  
PROPYLPARABEN  
PROPYLENE GLYCOL  
WATER  
SODIUM CITRATE  
SODIUM HYDROXIDE  
SODIUM LAURYL SULFATE  
SORBITAN MONOSTEARATE  
STEARIC ACID  
STEARYL ALCOHOL  
TROLAMINE  
UREA  
PETROLATUM  
Packaging
# Item Code Package Description
1 NDC:75854-102-04 1 TUBE, WITH APPLICATOR (TUBE) in 1 CARTON
1 4 g in 1 TUBE, WITH APPLICATOR
2 NDC:75854-102-24 24 TUBE, WITH APPLICATOR (TUBE) in 1 CARTON
2 4 g in 1 TUBE, WITH APPLICATOR
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 02/28/2008
Labeler - Avion Pharmaceuticals, LLC (965450542)
Revised: 10/2014
 
Avion Pharmaceuticals, LLC



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