Label: BISMUTH- bismuth subsalicylate suspension
- NDC Code(s): 13985-103-21
- Packager: MWI/VetOne
- 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.
If you are a consumer or patient please visit this version.
- NDC 13985-103-21 VET one Bismuth Suspension Anti-Diarrheal Liquid
For animal use only.
Keep out of reach of children.
Net Contents: 1 Gallon (3.785L)Close
Bismuth Subsalicylate ... 1.75%
In a palatable aqueous suspension. Flavoring and coloring added.Close
A palatable oral suspension for use as an aid in controlling simple diarrhea in cattle, horses, dogs and catsClose
This product contains salicylate; do not administer with other salicylate-containing products, such as aspirin.Close
- DOSAGE & ADMINISTRATION:
Shake well before using. Administer orally.
Dogs and Cats: 1 to 3 tablespoonfuls every 1-3 hours
Calves and Foals: 3 to 4 oz. every 2-3 hours
Cattle and Horses: 6 to 10 oz. every 2-3 hoursClose
If diarrhea persists after using this product for 2 days, contact a veterinarian.
FOR ORAL USE ONLY. SHAKE WELL BEFORE USING.Close
Store in a dry place at room temperature not above 37ºC (98.6ºF). Protect from freezing.
TAKE TIME OBSERVE LABEL DIRECTIONS
MADE IN USA Rev. 07/12
Distributed by: MWI
Boise, ID 83705Close
- PRINCIPAL DISPLAY PANEL
- INGREDIENTS AND APPEARANCE
bismuth subsalicylate suspension
Product Information Product Type OTC ANIMAL DRUG LABEL Item Code (Source) NDC:13985-103 Route of Administration ORAL DEA Schedule Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BISMUTH SUBSALICYLATE (BISMUTH CATION) BISMUTH SUBSALICYLATE 18 mg in 1 mL Inactive Ingredients Ingredient Name Strength GUAR GUM POTASSIUM SORBATE SACCHARIN SODIUM METHYL SALICYLATE WATER D&C RED NO. 33 SILICON DIOXIDE Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:13985-103-21 3785 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date Unapproved drug other 11/17/2010 Labeler - MWI/VetOne (019926120)