Label: BISMU-KOTE- bismuth subsalicylate suspension

  • Category: OTC ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated November 14, 2022

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  • PURPOSE

    Anti-Diarrheal Liquid
    Palatable Oral Suspension

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN
    FOR ANIMAL USE ONLY

  • 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 AND ADMINISTRATION:

    Administer orally.

    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 hours.

  • WARNING:

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

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  • ACTIVE INGREDIENT:

    Bismuth Subsalicylate........ 1.75% w/w
    In a palatable aqueous suspension.
    Flavoring and color added.

  • INACTIVE INGREDIENTS:

    Water, Xanthan Gum, Magnesium Salicylate, Methyl Salicylate, Sodium Saccharin, Hydrochloric Acid, Methylparaben, Propylparaben, and FD&C Red #40.

  • WHEN USING

    SHAKE WELL BEFORE USING.
    FOR ORAL USE ONLY
    KEEP FROM FREEZING.

  • STORAGE AND HANDLING

    Store at room temperature not above 37°C (98.6°F).

  • NET CONTENTS:

    1 GALLON (3.785 L)

  • INFORMATION FOR OWNERS/CAREGIVERS

    Distributed By
    VEDCO, INC.
    St. Joseph, MO 64507

    VINV-BSMO-KOTE

  • 1 GALLON (3.785 L)

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  • INGREDIENTS AND APPEARANCE
    BISMU-KOTE 
    bismuth subsalicylate suspension
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:50989-501
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BISMUTH SUBSALICYLATE (UNII: 62TEY51RR1) (SALICYLIC ACID - UNII:O414PZ4LPZ) BISMUTH SUBSALICYLATE17.4 g  in 1 L
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50989-501-294 in 1 CASE
    13.785 L in 1 JUG
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other04/09/2015
    Labeler - Vedco, Inc. (021634266)
    Establishment
    NameAddressID/FEIBusiness Operations
    First Priority Incorporated179925722manufacture, label, api manufacture
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