Label: BISMUTH- bismuth subsalicylate suspension

  • Category: OTC ANIMAL DRUG LABEL

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.

Drug Label Information

Updated September 17, 2013

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  • NDC 13985-103-21VET oneBismuthSuspensionAnti-Diarrheal Liquid    

    For animal use only.

    Keep out of reach of children.

    V1 510045

    Net Contents: 1 Gallon (3.785L)

  • CONTAINS:

    Bismuth Subsalicylate ... 1.75%

    In a palatable aqueous suspension. Flavoring and coloring added.

  • INDICATIONS:

    A palatable oral suspension for use as an aid in controlling simple diarrhea in cattle, horses, dogs and cats

  • CAUTION:

    This product contains salicylate; do not administer with other salicylate-containing products, such as aspirin.

  • 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 hours

  • WARNING:

    If diarrhea persists after using this product for 2 days, contact a veterinarian.

    FOR ORAL USE ONLY. SHAKE WELL BEFORE USING.

  • STORAGE:

    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 83705
    (888) 694-8381
    www.vetone.net

  • PRINCIPAL DISPLAY PANEL

    VetOne Bismuth Label

    Bottle Label

    Bottle Label

  • INGREDIENTS AND APPEARANCE
    BISMUTH 
    bismuth subsalicylate suspension
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:13985-103
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BISMUTH SUBSALICYLATE (UNII: 62TEY51RR1) (BISMUTH CATION - UNII:ZS9CD1I8YE) BISMUTH SUBSALICYLATE18 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    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)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:13985-103-213785 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    Unapproved drug other11/17/2010
    Labeler - MWI/VetOne (019926120)