Skip to Content

Readi-Cat

Generic Name: barium sulfate
Dosage Form: oral suspension

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.

NDC 32909-723-01
Readi-Cat® 2
BARIUM SULFATE SUSPENSION
(2.1% w/v, 2.0% w/w)

NDC 32909-725-03
BANANA SMOOTHIE
Readi-Cat® 2

NDC 32909-755-03
CREAMY VANILLA SMOOTHIE
Readi-Cat® 2

NDC 32909-715-03
BERRY SMOOTHIE
Readi-Cat® 2

NDC 32909-775-03
MOCHACCINO SMOOTHIE
Readi-Cat® 2

Readi-Cat Description

Readi-Cat® 2 is a barium sulfate suspension 2.1% w/v, 2.0% w/w for oral administration. Each 100 mL contains 2.1 g barium sulfate. Barium sulfate, due to its high molecular density is opaque to x-rays and therefore, acts as a positive contrast agent for radiographic studies. The active ingredient is barium sulfate and its structural formula is BaSO4. Barium sulfate occurs as a fine, white, odorless, tasteless, bulky powder which is free from grittiness. Its aqueous suspensions are neutral to litmus. It is practically insoluble in water, solutions of acids and alkalies, and organic solvents.

Inactive Ingredients
Citric acid, natural and artificial orange flavor, natural and artificial vanilla flavor, potassium sorbate, purified water, saccharin sodium, simethicone emulsion, sodium benzoate, sorbitol solution and xanthan gum.

BANANA SMOOTHIE Readi-Cat® 2 is a barium sulfate suspension 2.1% w/v, 2.0% w/w for oral administration. Each 100 mL contains 2.1 g barium sulfate. Barium sulfate, due to its high molecular density is opaque to x-rays and therefore, acts as a positive contrast agent for radiographic studies. The active ingredient is barium sulfate and its structural formula is BaSO4. Barium sulfate occurs as a fine, white, odorless, tasteless, bulky powder which is free from grittiness. Its aqueous suspensions are neutral to litmus. It is practically insoluble in water, solutions of acids and alkalies, and organic solvents.

Inactive Ingredients
Artificial vanilla flavor, benzoic acid, citric acid, natural banana flavor (with other natural flavors), potassium sorbate, purified water, saccharin sodium, simethicone emulsion, sodium benzoate, sodium citrate, sorbitol solution and xanthan gum.

CREAMY VANILLA SMOOTHIE Readi-Cat® 2 is a barium sulfate suspension 2.1% w/v, 2.0% w/w for oral administration. Each 100 mL contains 2.1 g barium sulfate. Barium sulfate, due to its high molecular density is opaque to x-rays and therefore, acts as a positive contrast agent for radiographic studies. The active ingredient is barium sulfate and its structural formula is BaSO4. Barium sulfate occurs as a fine, white, odorless, tasteless, bulky powder which is free from grittiness. Its aqueous suspensions are neutral to litmus. It is practically insoluble in water, solutions of acids and alkalies, and organic solvents.

Inactive Ingredients
Artificial vanilla flavor, benzoic acid, citric acid, potassium sorbate, purified water, saccharin sodium, simethicone emulsion, sodium benzoate, sodium citrate, sorbitol solution and xanthan gum.

BERRY SMOOTHIE Readi-Cat® 2 is a barium sulfate suspension 2.1% w/v, 2.0% w/w for oral administration. Each 100 mL contains 2.1 g barium sulfate. Barium sulfate, due to its high molecular density is opaque to x-rays and therefore, acts as a positive contrast agent for radiographic studies. The active ingredient is barium sulfate and its structural formula is BaSO4. Barium sulfate occurs as a fine, white, odorless, tasteless, bulky powder which is free from grittiness. Its aqueous suspensions are neutral to litmus. It is practically insoluble in water, solutions of acids and alkalies, and organic solvents.

Inactive Ingredients
Benzoic acid, citric acid, natural and artificial blueberry flavor, potassium sorbate, purified water, saccharin sodium, simethicone emulsion, sodium benzoate, sodium citrate, sorbitol solution and xanthan gum.

MOCHACCINO SMOOTHIE Readi-Cat® 2 is a barium sulfate suspension 2.1% w/v, 2.0% w/w for oral administration. Each 100 mL contains 2.1 g barium sulfate. Barium sulfate, due to its high molecular density is opaque to x-rays and therefore, acts as a positive contrast agent for radiographic studies. The active ingredient is barium sulfate and its structural formula is BaSO4. Barium sulfate occurs as a fine, white, odorless, tasteless, bulky powder which is free from grittiness. Its aqueous suspensions are neutral to litmus. It is practically insoluble in water, solutions of acids and alkalies, and organic solvents.

Inactive Ingredients
Benzoic acid, citric acid, natural and artificial bavarian chocolate flavor, natural and artificial coffee cappuccino flavor, potassium sorbate, purified water, saccharin sodium, simethicone emulsion, sodium benzoate, sodium citrate, sorbitol solution and xanthan gum.

CLINICAL PHARMACOLOGY

Barium sulfate, due to its high molecular density is opaque to x-rays and, therefore, acts as a positive contrast agent for radiographic studies. Barium sulfate is biologically inert and, therefore, is not absorbed or metabolized by the body, and is eliminated from the GI tract unchanged.

INDICATIONS AND USAGE

For use in Computed Tomography to opacify the GI tract.

Contraindications

This product should not be used in patients with known or suspected gastric or intestinal perforation, or hypersensitivity to barium sulfate or any component of this barium sulfate formulation.

Warnings

Rarely, severe allergic reactions of an anaphylactoid nature, have been reported following administration of barium sulfate contrast agents. Appropriately trained personnel and facilities should be available for emergency treatment of severe reactions and should remain available for at least 30 to 60 minutes following administration, since delayed reactions can occur.

Precautions

General

Diagnostic procedures which involve the use of radiopaque contrast agents should be carried out under the direction of personnel with the requisite training and with a thorough knowledge of the particular procedure to be performed. A history of bronchial asthma, atopy, as evidenced by hay fever and eczema, or a previous reaction to a contrast agent, warrant special attention. Caution should be exercised with the use of radiopaque media in severely debilitated patients and in those with marked hypertension or advanced cardiac disease. Ingestion of barium is not recommended in patients with a history of food aspiration. If barium studies are required in these patients or in patients in whom integrity of the swallowing mechanism is unknown, proceed with caution. If barium is aspirated into the larynx, further administration should be immediately discontinued. After any barium study of the GI tract, it is important to rehydrate the patient as quickly as possible to prevent impaction of the barium. To prevent barium impaction in the colon, the use of mild laxatives such as milk of magnesia or lactulose following completion of the examination may also be required. These mild laxatives are recommended on a routine basis and in patients with a history of constipation unless clinically contraindicated.

Information for Patients

Before using this product patients should be instructed to tell the physician ordering the procedure and the imaging technologist:

  1. if they are pregnant.
  2. if they are allergic to any foods or medication, or if they have had any prior reactions to barium sulfate products or other x-ray contrast agents.
  3. if they are currently taking any medications, have any serious medical condition for which they are being treated or followed, or had any recent surgery.
  4. seek immediate medical attention if they experience an allergic reaction after using this product.

Drug Interactions

The presence of barium sulfate formulations in the GI tract may alter the absorption of therapeutic agents taken concomitantly. In order to minimize any potential change in absorption, the separate administration of barium sulfate from that of other agents should be considered.

Usage in Pregnancy

Radiation is known to cause harm to the unborn fetus exposed in utero. Therefore, radiographic procedures should only be used when, in the judgement of the physician, its use is deemed essential to the welfare of the pregnant patient.

Nursing Mothers

Barium sulfate products may be used during lactation.

ADVERSE REACTIONS

Adverse reactions, such as nausea, vomiting, diarrhea and abdominal cramping, accompanying the use of barium sulfate formulations are infrequent and usually mild. Severe reactions (approximately 1 in 1,000,000) and fatalities (approximately 1 in 10,000,000) have occurred. Procedural complications are rare, but may include aspiration pneumonitis, barium impaction, granuloma formation, intravasation, embolization and peritonitis following intestinal perforation, vasovagal and syncopal episodes, and fatalities. EKG changes have been reported following or during barium enema procedures. It is of the utmost importance to be completely prepared to treat any such occurrence.

ALLERGIC REACTIONS

Due to the increased likelihood of allergic reactions in atopic patients, it is important that a complete history of known and suspected allergies as well as allergiclike symptoms, e.g., rhinitis, bronchial asthma, eczema and urticaria, must be obtained prior to any medical procedure utilizing these products. A mild allergic reaction would most likely include generalized pruritus, erythema or urticaria (approximately 1 in 250,000). Such reactions will generally respond to an antihistamine such as 50 mg of diphenhydramine or its equivalent. In the rarer, more serious reactions (approximately 1 in 1,000,000) laryngeal edema, bronchospasm or hypotension could develop. Severe reactions which may require emergency measures are often characterized by peripheral vasodilation, hypotension, reflex tachycardia, dyspnea, agitation, confusion and cyanosis, progressing to unconsciousness. Treatment should be initiated immediately with 0.3 to 0.5 cc of 1:1000 epinephrine subcutaneously. If bronchospasm predominates, 0.25 to 0.50 grams of intravenous aminophylline should be given slowly. Appropriate vasopressors might be required. Adrenocorticosteroids, even if given intravenously, exert no significant effect on the acute allergic reactions for a few hours. The administration of these agents should not be regarded as emergency measures for the treatment of allergic reactions.

Apprehensive patients may develop weakness, pallor, tinnitus, diaphoresis and bradycardia following the administration of any diagnostic agent. Such reactions are usually non-allergic in nature and are best treated by having the patient lie flat for an additional 10 to 30 minutes under observation.

Overdosage

On rare occasions following repeated administration, severe stomach cramps, nausea, vomiting, diarrhea or constipation may occur. These indicated responses can be present in both fluoroscopic and CT procedures. These are transitory in nature and are not considered serious. Symptoms may be treated according to currently accepted standards of medical care.

DOSAGE AND ADMINISTRATION

The volume and concentration of the CT barium sulfate suspension to be administered will depend on the degree and extent of contrast required in the area(s) under examination and on the equipment and technique employed.

Suggested 30 Minute Barium Administration Protocol for Abdomen Studies:
Administer 300 mL CT barium suspension 30 minutes before scan and 150 mL immediately prior to scan; or use as directed by physician.

Suggested 90 Minute Barium Administration Protocol for Abdomen/Pelvis Studies: Administer 450 mL CT barium suspension 90 minutes before scan, another 300 mL 30 minutes before scan, and finally 150 mL immediately prior to scan; or use as directed by physician.
Other dosing regimens may be followed as applicable.

STORAGE

USP Controlled Room Temperature, 20 to 25°C (68 to 77°F). Protect from freezing.

How is Readi-Cat Supplied

Readi-Cat® 2 is supplied in the following quantities:
450 mL bottles, Cat. No. 723, NDC 32909-723-01.

BANANA SMOOTHIE Readi-Cat® 2 is supplied in the following quantities:
450 mL bottles, Cat. No. 7450, NDC 32909-725-03.

CREAMY VANILLA SMOOTHIE Readi-Cat® 2 is supplied in the following quantities:
450 mL bottles, Cat. No. 7550, NDC 32909-755-03.

BERRY SMOOTHIE Readi-Cat® 2 is supplied in the following quantities:
450 mL bottles, Cat. No. 7150, NDC 32909-715-03.

MOCHACCINO SMOOTHIE Readi-Cat® 2 is supplied in the following quantities:
450 mL bottles, Cat. No. 450307, NDC 32909-775-03.




SHAKE WELL PRIOR TO USE



Manufactured by E-Z-EM Canada Inc.
for E-Z-EM, Inc., a subsidiary of Bracco Diagnostics Inc.
Monroe Township, NJ 08831
Tel. 1-516-333-8230 1-800 544-4624

rev. 11/13 TX1665-1



Readi–Cat® 2 Barium Sulfate Suspension
CAT. NO. 723
NDC: 32909–723–01

Readi–Cat® 2 Barium Sulfate Suspension
CAT. NO. 7150
NDC: 32909–715–03

Readi–Cat® 2 Barium Sulfate Suspension
CAT. NO. 7450
NDC: 32909–725–03

Readi–Cat® 2 Barium Sulfate Suspension
CAT. NO. 7550
NDC: 32909–755–03

Readi–Cat® 2 Barium Sulfate Suspension
CAT NO. 450307
NDC: 32909–775–03

Readi-Cat2 
barium sulfate suspension
Product Information
Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:32909-723
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Barium Sulfate (Barium Sulfate) Barium Sulfate 21 mg  in 1 mL
Inactive Ingredients
Ingredient Name Strength
anhydrous citric acid  
dimethicone 350  
dimethicone 1000  
potassium sorbate  
saccharin sodium dihydrate  
silicon dioxide  
sodium benzoate  
sorbitol  
water  
xanthan gum  
Product Characteristics
Color WHITE Score     
Shape Size
Flavor ORANGE Imprint Code
Contains         
Packaging
# Item Code Package Description
1 NDC:32909-723-01 450 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
Unapproved drug other 06/01/1985
Readi-Cat2 BANANA SMOOTHIE 
barium sulfate suspension
Product Information
Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:32909-725
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Barium Sulfate (Barium Sulfate) Barium Sulfate 21 mg  in 1 mL
Inactive Ingredients
Ingredient Name Strength
anhydrous citric acid  
benzoic acid  
dimethicone 350  
dimethicone 1000  
potassium sorbate  
saccharin sodium dihydrate  
silicon dioxide  
sodium benzoate  
trisodium citrate dihydrate  
sorbitol  
water  
xanthan gum  
Product Characteristics
Color WHITE Score     
Shape Size
Flavor BANANA, VANILLA Imprint Code
Contains         
Packaging
# Item Code Package Description
1 NDC:32909-725-03 450 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
Unapproved drug other 08/01/1998
Readi-Cat2 BERRY SMOOTHIE 
barium sulfate suspension
Product Information
Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:32909-715
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Barium Sulfate (Barium Sulfate) Barium Sulfate 21 mg  in 1 mL
Inactive Ingredients
Ingredient Name Strength
anhydrous citric acid  
benzoic acid  
dimethicone 350  
dimethicone 1000  
potassium sorbate  
saccharin sodium dihydrate  
silicon dioxide  
sodium benzoate  
trisodium citrate dihydrate  
sorbitol  
water  
xanthan gum  
Product Characteristics
Color WHITE Score     
Shape Size
Flavor BLUEBERRY Imprint Code
Contains         
Packaging
# Item Code Package Description
1 NDC:32909-715-03 450 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
Unapproved drug other 02/01/2002
Readi-Cat2 MOCHACCINO SMOOTHIE 
barium sulfate suspension
Product Information
Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:32909-775
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Barium Sulfate (Barium Sulfate) Barium Sulfate 21 mg  in 1 mL
Inactive Ingredients
Ingredient Name Strength
anhydrous citric acid  
benzoic acid  
dimethicone 350  
dimethicone 1000  
potassium sorbate  
saccharin sodium dihydrate  
silicon dioxide  
sodium benzoate  
trisodium citrate dihydrate  
sorbitol  
water  
xanthan gum  
Product Characteristics
Color WHITE Score     
Shape Size
Flavor COFFEE, CHOCOLATE Imprint Code
Contains         
Packaging
# Item Code Package Description
1 NDC:32909-775-03 450 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
Unapproved drug other 03/31/2009
Readi-Cat2 VANILLA SMOOTHIE 
barium sulfate suspension
Product Information
Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:32909-755
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Barium Sulfate (Barium Sulfate) Barium Sulfate 21 mg  in 1 mL
Inactive Ingredients
Ingredient Name Strength
anhydrous citric acid  
benzoic acid  
dimethicone 350  
dimethicone 1000  
potassium sorbate  
saccharin sodium dihydrate  
silicon dioxide  
sodium benzoate  
trisodium citrate dihydrate  
sorbitol  
water  
xanthan gum  
Product Characteristics
Color WHITE Score     
Shape Size
Flavor VANILLA Imprint Code
Contains         
Packaging
# Item Code Package Description
1 NDC:32909-755-03 450 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
Unapproved drug other 11/01/2005
Labeler - E-Z-EM Canada Inc (204211163)
Registrant - E-Z-EM, INC. (002041226)
Establishment
Name Address ID/FEI Operations
Cimbar Performance Minerals, Inc. 963805671 API MANUFACTURE(32909-755, 32909-715, 32909-775, 32909-725, 32909-723)
Establishment
Name Address ID/FEI Operations
E-Z-EM Canada Inc 204211163 LABEL(32909-723, 32909-725, 32909-715, 32909-775, 32909-755), ANALYSIS(32909-725, 32909-723, 32909-755, 32909-775, 32909-715), MANUFACTURE(32909-723, 32909-755, 32909-715, 32909-775, 32909-725), PACK(32909-723, 32909-715, 32909-775, 32909-755, 32909-725)
Revised: 03/2014
 
E-Z-EM Canada Inc
Hide