Label: KAOLIN-PECTIN suspension

  • NDC Code(s): 58005-501-50
  • Packager: Sparhawk Laboratories, Inc
  • Category: OTC ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated February 9, 2017

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  • INDICATIONS & USAGE

    ANTI-DIARRHEAL LIQUID

    FOR ANIMAL USE ONLY

    KEEP OUT OF REACH OF CHILDREN

    INDICATIONS

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

  • DOSAGE AND ADMINISTRATION

    Administer orally after first sign of diarrhea and after each loose bowel movement or as needed.

    Cattle and Horses:  6 to 10 fl. ozs.

    Calves and Foals:   3 to 4 fl. ozs.

    Dogs and Cats:  1 to 3 tablespoons


  • WARNING

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

  • COMPONENTS

    EACH FLUID OUNCE CONTAINS

    ACTIVE INGREDIENTS

    Kaolin (colloidal) ................................ 90 gr.
    Pectin (citrus) .................................... 2 gr.

    Inactive Ingredients:  Guar Gum, Dextrose Monohydrate, Wild Cherry Flavor, Disodium Edetate, Methyl Paraben, Propyl Paraben, Sodium Carbonate, Sorbitol - 70%, Vanilla Flavor, FDC Red #40 Lake, and Water for Injection.

  • STORAGE AND HANDLING

    SHAKE WELL BEFORE USING

    PROTECT FROM FREEZING.

    TAKE TIME OBSERVE LABEL DIRECTIONS.

  • PRINCIPAL DISPLAY PANEL

    SLI Kaolin Pectin

  • INGREDIENTS AND APPEARANCE
    KAOLIN-PECTIN 
    kaolin-pectin suspension
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:58005-501
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    KAOLIN (UNII: 24H4NWX5CO) (KAOLIN - UNII:24H4NWX5CO) KAOLIN5.8 g  in 29.57 mL
    PECTIN (UNII: 89NA02M4RX) (PECTIN - UNII:89NA02M4RX) PECTIN0.13 g  in 29.57 mL
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorCHERRY (CHERRY FLAVOR) , VANILLA (VANILLA FLAVOR) Imprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:58005-501-503785 mL in 1 JUG
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other08/11/1995
    Labeler - Sparhawk Laboratories, Inc (147979082)
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