Label: HEMOSTAT- iron powder

  • NDC Code(s): 57319-392-21
  • Packager: Clipper Distributing Company, LLC
  • Category: OTC ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated June 26, 2017

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  • INDICATIONS & USAGE

    CONTROLS MINOR BLEEDING

    FOR ANIMAL USE ONLY

    KEEP OUT OF REACH OF CHILDREN

    INDICATIONS

    For use as an aid in controlling minor bleeding from superficial cuts and wounds and after dehorning.

  • DOSAGE AND ADMINISTRATION

    Apply powder freely to bleeding surface.  Repeat as needed. Bandage if necessary.

  • CONTRAINDICATIONS

    In case of deep or puncture wounds or serious burns, consult veterinarian. If redness, irritation, or swelling persists or increases, discontinue use and consult veterinarian.

  • COMPOSITION

    Ferrous Sulfate • 7H2O 84.0%, Ammonium Alum 5%, Chloroxylenol 1%, Tannic Acid 1%, In a free-flowing absorbent base. Not sterilized

    For external use only.

  • STORAGE AND HANDLING

    Store at controlled room temperature between 15° and 30°C (59°-86°F)

    Keep container tightly closed.

    TAKE TIME OBSERVE LABEL DIRECTIONS

  • PRINCIPAL DISPLAY PANEL

    PX Blood Stop Powder

  • INGREDIENTS AND APPEARANCE
    HEMOSTAT 
    iron powder
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:57319-392
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    FERROUS SULFATE (UNII: 39R4TAN1VT) (FERROUS CATION - UNII:GW89581OWR) FERROUS CATION76.6 g  in 454 g
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:57319-392-21454 g in 1 JAR
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other02/07/2009
    Labeler - Clipper Distributing Company, LLC (150711039)
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