Label: ISOPROPYL ALCOHOL- isopropyl alcohol liquid

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

Drug Label Information

Updated 09/13

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  • NDC 30798-786-35 durvet 70% ALCOHOL SOLUTION Contains 70% Isopropyl Alcohol

    Rubefacient

    www.durvet.com

    NET CONTENTS: ONE GALLON (3.785 L)

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  • FOR ANIMAL USE ONLY

    INDICATIONS: Helps relieve minor muscular aches due to overexertion.

    DIRECTIONS: Apply liberally and rub in.

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  • CAUTION:

    Harmful if swallowed.

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  • WARNING:

    FOR EXTERNAL USE ONLY.  Keep out of reach of children.  If taken internally, severe gastric disturbances will result.  In case of accidental ingestion, call a physician or poison control center immediately.  Causes eye irritation.  In case of contact, immediately flush eyes with water and call a physician.  May cause skin irritation.  Avoid contact with eyes, skin, mucous membranes and clothing.  Wash hands thoroughly after handling.

    TAKE TIME OBSERVE LABEL DIRECTIONS

    Manufactured for:

    DURVET, INC.

    Blue Springs, Missouri 64014

    Iss. 07-09

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  • KEEP OUT OF REACH OF CHILDREN
  • CONTENTS:

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

    Purified Water .................... 30%

    This preparation is made from Isopropyl Alcohol and does not contain, nor is it sold as a substitute for, ethyl or grain alcohol.

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  • STORAGE:

    Store at controlled room temperature between 15º - 30ºC (59º-86ºF).  Keep tightly closed, protect from light.

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  • WARNING!  FLAMMABLE!

    KEEP AWAY FROM HEAT AND OPEN FLAME

    Lot No.          Exp. Date´╗┐

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  • DESCRIPTION

    Label

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  • INGREDIENTS AND APPEARANCE
    ISOPROPYL ALCOHOL 
    isopropyl alcohol liquid
    Product Information
    Product Type OTC ANIMAL DRUG Item Code (Source) NDC:30798-786
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 70 mL  in 100 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:30798-786-35 3785 mL in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    Unapproved drug other 08/10/2009
    Labeler - Durvet, Inc. (056387798)
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