Label: ISOPROPYL ALCOHOL 99%- isopropyl alcohol 99% 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 November 14, 2018

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  • DOSAGE & ADMINISTRATION

    Topical

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  • INACTIVE INGREDIENT

    Purified Water

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  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

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  • ACTIVE INGREDIENT

    Isopropyl Alcohol Anhydrous not less than 99% by volume.

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  • WARNINGS

    Keep away from spark, heat, or flame

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  • INDICATIONS & USAGE

    Use as a solvent for cleaning gums, shellac, and essential oils.

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  • PURPOSE

    Solvent

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  • INGREDIENTS AND APPEARANCE
    ISOPROPYL ALCOHOL 99% 
    isopropyl alcohol 99% liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:70677-0045
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 990 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R) 1 mg  in 1 mL
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:70677-0045-1 473 mL in 1 CONTAINER; Type 0: Not a Combination Product 07/01/2018
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333A 07/01/2018
    Labeler - McKesson Drug Company (177667227)
    Registrant - Humco Holding Group, Inc. (825672884)
    Establishment
    Name Address ID/FEI Business Operations
    Humco Holding Group, Inc. 825672884 manufacture(70677-0045) , pack(70677-0045)
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