Label: ETHYL RUBBING ALCOHOL- alcohol liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated June 5, 2011

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENT

    CONTAINS:70% Ethyl Alcohol by volume

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  • PURPOSE

    INDICATIONS. To decrease germs in minor cuts and scrapes

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  • DOSAGE & ADMINISTRATION

    DIRECTIONS. Apply to skin directly or with clean gauze cotton or swab  For rubbing apply  liberally and rub with hands.

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  • WARNINGS

    WARNINGS.FOR EXTERNAL USE ONLY Will produce serious gastric disturbances if taken internally

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  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF THE REACH OF CHILDREN. In case of accidental ingestion seek professional assistance or contact a Poison Control Center inmediately

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  • INDICATIONS & USAGE

    CAUTION Do not apply to irritated skin use in eyes or on mucous membranes incase of deep or puncture wounds consult a doctor

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  • INACTIVE INGREDIENT

    INACTIVE INGREDIENTS .Denatonium Benzoate water

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  • PRINCIPAL DISPLAY PANEL

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  • INGREDIENTS AND APPEARANCE
    ETHYL RUBBING ALCOHOL 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:15231-100
    Route of AdministrationCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R) 29.65 mL  in 100 mL
    DENATONIUM BENZOATE ANHYDROUS (UNII: M5BA6GAF1O) .35 mg  in 100 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:15231-100-01500 mL in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E02/09/1998
    Labeler - COMERCIALIZADORA JIQUILPAN S.A. DE C.V. (589780068)
    Establishment
    NameAddressID/FEIBusiness Operations
    COMERCIALIZADORA JIQUILPAN S.A. DE C.V.589780068manufacture