Label: ISOPROPYL ALCOHOL liquid

  • NDC Code(s): 57319-430-09, 57319-430-22
  • Packager: Phoenix Pharmaceutical Inc./ Clipper Distributing, Inc.
  • Category: OTC ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Updated September 17, 2013

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  • NDC 57319-430-09Isopropyl Alcohol 70%FOR EXTERNAL USE ONLYKEEP OUT OF REACH OF CHILDREN   

    NET CONTENTS:

    3.785L (1 GALLON)

    PHOENIXTM

    PHARMACEUTICAL, INC.

    Manufactured for:

    Clipper Distributing Company, LLC

    St. Joseph, MO 64507

  • For Veterinary Use Only

    Scrub hands and arms with soap and water, rinse with water, then scrub with alcohol solution for disinfecting.

    External Solution for use as a topical antiseptic. may also be used for temporary relief of minor muscular aches or pain due to overexertion and fatigue. Apply full strength directly to affected area, wet thoroughly and massage briskly to stimulate circulation.

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

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

    Rev. 10-09

    TAKE TIME OBSERVE LABEL DIRECTIONS

    Trademarks are property of
    Clipper Distributing Company, LLC

  • ACTIVE INGREDIENT

    ACTIVE INGREDIENT:

    Isopropyl Alcohol ................ 70%

  • INACTIVE INGREDIENT

    INERT INGREDIENT

    Deionized Water ................. 30%
    Total ................................. 100%

  • WARNING

    For external use only. If taken internally, serious gastric disturbance will result. Avoid contact with eyes. In case of eye contact, flush thoroughly with water. Call a physician.

    First Aid:

    Induce vomiting or use stomach pump.

  • CAUTION

    FLAMMABLE
    KEEP AWAY FROM FIRE OR FLAME

    KEEP CONTAINER CLOSED WHEN NOT IN USE

  • PRINCIPAL DISPLAY PANEL

    Phoenix IPA 70 bottle label

  • INGREDIENTS AND APPEARANCE
    ISOPROPYL ALCOHOL 
    isopropyl alcohol liquid
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:57319-430
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:57319-430-22946 mL in 1 BOTTLE
    2NDC:57319-430-093785 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    Unapproved drug other01/29/2002
    Labeler - Phoenix Pharmaceutical Inc./ Clipper Distributing, Inc. (150711039)
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