Label: KAOLIN PECTIN- kaolin-pectin suspension

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

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 April 25, 2018

If you are a consumer or patient please visit this version.

  • INDICATIONS & USAGE

    FOR ANIMAL USE ONLY

    ANTI-DIARRHEAL LIQUID

    KEEP OUT OF REACH OF CHILDREN

    INDICATIONS

    For use as an aid in the relief of simple (uncomplicated) diarrhea and gastroenteritis.

  • 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 Foals3 to 4 fl. ozs.

    Dogs and Cats 1 to 3 tablespoonfuls

  • WARNINGS

    If symptoms persist after using this product for 2 or 3 days, the diagnosis and appropriate treatment should be reconsidered. 

  • COMPOSITION

    Each fluid ounce (2 tablespoonfuls) contains:

    Kaolin ................................ 90 gr. (5.8 g)

    Pectin ................................ 2 gr. (0.13 g)

    In a palatable vehicle.

    Flavorings and color added.

  • STORAGE AND HANDLING

    Store in controlled room temperature between 15° and 30° (59°-86°).

    Protect from freezing.

    SHAKE WELL BEFORE USING

    TAKE TIME OBSERVE LABEL DIRECTIONS

  • PRINCIPAL DISPLAY PANEL

    VED Kaolin Pectin

  • INGREDIENTS AND APPEARANCE
    KAOLIN PECTIN 
    kaolin-pectin suspension
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:50989-062
    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
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50989-062-293785 mL in 1 JUG
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other07/06/1998
    Labeler - Vedco, Inc. (021634266)