Label: CORRECTIVE- bismuth subsalicylate suspension

  • NDC Code(s): 57319-393-09
  • Packager: Phoenix Pharmaceutical Inc./ Clipper Distributing, Inc.
  • Category: OTC ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated September 17, 2013

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  • NDC 57319-393-09Corrective SuspensionAnti-Diarrheal Suspension  

    FOR ANIMAL USE ONLY

    KEEP OUT OF REACH OF CHILDREN

    Net Contents:

    3.785L (1 Gal.)

    Manufactured For:

    PHOENIX

    PHARMACEUTICAL, INC.

    St. Joseph, MO 64503

  • INDICATIONS:

    For oral administration as an aid in the treatment of noninfectious diarrhea in horses, cattle, dogs and cats.

  • DOSAGE:

    Cattle 6 - 10 oz. Every 2 - 3 hours
    Calves 3 - 4 oz. Every 2 - 3 hours
    Horses 6 - 10 oz. Every 2 - 3 hours
    Foals 3 - 4 oz. Every 2 - 3 hours
    Dogs 1 - 3 Tbls. (1/2 - 2 oz.) Every 1 - 3 hours
    Cats 1 - 3 Tbls. (1/2 - 2 oz.) Every 1 - 3 hours

  • WARNING:

    If symptoms persist after using this product for 2 to 3 days consult a veterinarian.

    FOR ANIMAL USE ONLY

    NOT FOR HUMAN USE

    Rev 11-01

    Lot No.

    Exp. Date

  • CONTAINS:

    Bismuth Subsalicylate ........... 1.75%

    Administration: Oral.

  • SHAKE WELL BEFORE USING.KEEP FROM FREEZING.

  • KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN

    TAKE TIME OBSERVE LABEL DIRECTIONS

    Manufactured by:
    Ameri-Pac
    St. Joseph, MO 64502

  • PRINCIPAL DISPLAY PANEL

    Bottle Label

  • INGREDIENTS AND APPEARANCE
    CORRECTIVE 
    bismuth subsalicylate suspension
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:57319-393
    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
    WATER (UNII: 059QF0KO0R)  
    GUAR GUM (UNII: E89I1637KE)  
    METHYL SALICYLATE (UNII: LAV5U5022Y)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorWINTERGREENImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:57319-393-093785 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    Unapproved drug other04/20/2000
    Labeler - Phoenix Pharmaceutical Inc./ Clipper Distributing, Inc. (150711039)
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