Label: SCARLET OIL WOUND DRESSING- scarlet oil solution

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

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Drug Label Information

Updated November 10, 2022

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  • PURPOSE

    For Simple Wounds, Cuts and Abrasions

  • ACTIVE INGREDIENT

    Active Ingredient 0.3% (w/w) PCMX (Parachlorometaxylenol)

  • WHEN USING

    FOR ANIMAL USE ONLY

  • INDICATIONS:

    For use as a dressing for simple wounds, cuts and abrasions on horses and mules.

  • CAUTION:

    Use only as directed. Avoid contact with eyes and mucous membranes. Do not apply to large areas of broken skin. In case of deep or puncture wounds or serious burns, consult a veterinarian. If redness, irritation, or swelling persists or increases, discontinue use and consult a veterinarian.

  • DIRECTIONS FOR USE:

    Clean the affected area, clipping hair if necessary. Direct spray at the site to be treated. Hold container 4 to 6 inches from animal. Apply freely as an open wound treatment or wrap with a clean bandage. Treatment may be applied once or twice daily.

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  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN

  • INACTIVE INGREDIENTS:

    Mineral Oil, Isopropyl Alcohol, Methyl Salicylate, Benzyl Alcohol, Pine Oil, Eucalyptus Oil and Scarlet Red.

  • FOOD SAFETY WARNING

    WARNING: Not for use on animals intended for food.

  • STORAGE:

    Store at controlled room temperature between 15º-30ºC (59º-86ºF). Keep container tightly closed when not in use.

  • WARNINGS AND PRECAUTIONS

    WARNING! FLAMMABLE! KEEP AWAY FROM HEAT AND OPEN FLAME.

  • Net Contents:

    16 OZ (473 mL)

  • INFORMATION FOR OWNERS/CAREGIVERS

    Manufactured for:
    DURVET, INC.
    Blue Springs, Missouri 64014    Rev. 04-16

    www.durvet.com

  • Net Contents: 16 fl oz (473 mL)

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  • INGREDIENTS AND APPEARANCE
    SCARLET OIL  WOUND DRESSING
    scarlet oil solution
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:30798-626
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL2.5 mg  in 1 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:30798-626-3112 in 1 CASE
    1473 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other04/06/2015
    Labeler - Durvet, Inc. (056387798)
    Establishment
    NameAddressID/FEIBusiness Operations
    FIRST PRIORITY INCORPORATED179925722manufacture, label
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