Label: ISOPROPYL ALCOHOL liquid

  • 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 September 20, 2013

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  • NDC 30798-786-35durvet70% ALCOHOL SOLUTIONContains 70% Isopropyl Alcohol

    Rubefacient

    www.durvet.com

    NET CONTENTS: ONE GALLON (3.785 L)

  • FOR ANIMAL USE ONLY

    INDICATIONS: Helps relieve minor muscular aches due to overexertion.

    DIRECTIONS: Apply liberally and rub in.

  • CAUTION:

    Harmful if swallowed.

  • 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

  • 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.

  • STORAGE:

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

  • WARNING!  FLAMMABLE!

    KEEP AWAY FROM HEAT AND OPEN FLAME

    Lot No.          Exp. Date

  • DESCRIPTION

    Label

  • PRINCIPAL DISPLAY PANEL

    Durvet 70 Alcohol Solution 3.785L

  • INGREDIENTS AND APPEARANCE
    ISOPROPYL ALCOHOL 
    isopropyl alcohol liquid
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:30798-786
    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:30798-786-353785 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    Unapproved drug other08/10/2009
    Labeler - Durvet, Inc. (056387798)