Label: HUMCO ISOPROPYL RUBBING ALCOHOL 70% PROFESSIONAL PACK- isopropyl alcohol liquid

  • NDC Code(s): 0395-4202-28
  • Packager: Humco Holding Group, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 15, 2023

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient

    Isopropyl Alcohol 70% by volume

  • Purpose

    First aid antiseptic

  • Use

    First aid to help prevent the risk of infection in.

    • minor cuts
    • scrapes
    • burns
  • Warnings

    For external use only.

    • Flammable, keep way from spark, heat and flame.
  • Ask a doctor before use for

    • deep wounds
    • animal bites
    • serious burns
  • When using this product

    • do not get into eyes
    • do not apply over large areas of the body
    • do not use longer than 1 week
  • Stop use and ask a doctor if

    condition persists or gets worse

  • Keep out of reach of children.

    In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

  • Directions

    • clean the affected area.
    • apply a smal amount of this product on the affected area 1 to 3 times daily.
    • may be covered with sterile bandage.
    • if bandaged, let it dry first.
  • Other Information

    • store at room temperature
    • does not contain, nor is intended as a substitute for grain or ethyl alcohol.
    • will produce serious gastric distrurbances if taken internally.
  • Inactive Ingredient

    purified water

  • Principal Package Display Pannel

    IPA 70 Gal Propack.jpgimage description

    Label

  • INGREDIENTS AND APPEARANCE
    HUMCO ISOPROPYL RUBBING ALCOHOL 70% PROFESSIONAL PACK 
    isopropyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0395-4202
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL700 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0395-4202-283800 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/14/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00303/25/1998
    Labeler - Humco Holding Group, Inc. (825672884)
    Registrant - Pharma Nobis, LLC (118564114)
    Establishment
    NameAddressID/FEIBusiness Operations
    Pharma Nobis, LLC118564114label(0395-4202) , manufacture(0395-4202) , analysis(0395-4202) , pack(0395-4202)
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