Label: BISMUTH- bismuth subsalicylate suspension
- NDC Code(s): 50989-527-29
- Packager: VEDCO
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
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- NDC 50989-527-29 BISMU-KOTE ANTI-DIARRHEAL LIQUID PALATABLE ORAL SUSPENSION
NET CONTENTS: 1 GALLON (3.785 L)
KEEP OUT OF REACH OF CHILDREN
FOR ANIMAL USE ONLYClose
A palatable oral suspension for use as an aid in controlling simple diarrhea in cattle, horses, dogs and cats.Close
This product contains salicylate; do not administer with other salicylate-containing products, such as aspirin.Close
- DOSAGE AND ADMINISTRATION:
Dogs and Cats- 1 to 3 tablespoonfuls every 1-3 hours
Calves and Foals- 3 to 4 ounces every 2-3 hours
Horses and Cattle- 6 to 10 ounces every 2-3 hoursClose
If diarrhea persists after using this product for 2 days, contact a veterinarian.
St. Joseph, MO 64504Close
In a palatable aqueous suspension.
Flavoring and coloring added.
SHAKE WELL BEFORE USING.
FOR ORAL USE ONLY
KEEP FROM FREEZING.Close
- STORAGE AND HANDLING
Store at room temperature above 37ºC (98.6ºF).
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- INGREDIENTS AND APPEARANCE
bismuth subsalicylate suspension
Product Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:50989-527 Route of Administration ORAL DEA Schedule Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BISMUTH SUBSALICYLATE (UNII: 62TEY51RR1) (BISMUTH CATION - UNII:ZS9CD1I8YE) BISMUTH SUBSALICYLATE 18 mg in 1 mL Inactive Ingredients Ingredient Name Strength GUAR GUM (UNII: E89I1637KE) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) SACCHARIN SODIUM (UNII: SB8ZUX40TY) METHYL SALICYLATE (UNII: LAV5U5022Y) WATER (UNII: 059QF0KO0R) D&C RED NO. 33 (UNII: 9DBA0SBB0L) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) Product Characteristics Color pink Score Shape Size Flavor WINTERGREEN Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50989-527-29 3785 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date Unapproved drug other 03/27/2000 Labeler - VEDCO (021634266)