Label: GNP ISOPROPYL ALCOHOL 70 PERCENT WITH WINTERGREEN OIL- isopropyl alcohol liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 14, 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.
    • Use in well ventilated area, fumes may be harmful.
  • Ask a doctor before use for

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

    • do not get into eyes or mucous membranes.
    • do not apply to irritated skin.
  • Stop use and ask a doctor if

    excessive irritation of the skin develops.

  • Keep out of reach of children.

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

  • Directions

    • apply freely and rub briskly with hands or towel.
  • Other Information

    • does not contain ethyl or grain alcohol and is not sold as a substitute for preparations containing the same.
    • Store at controlled room temperature
    • will produce serious gastric disturbances if taken internally.
  • Inactive Ingredient

    Methyl salicylate 0.5%

    FDC Blue #1

    FDC Yellow #5

    purified water

  • Principal Display Panel

    GNP70W.jpgNDC 46122-331-43

    ISOPROPYL

    RUBBING

    ALCOHOL 7 0%

    With Wintergreen Oil

    Rubbing, Massage, Sponge Bath

    16 fl oz (1 pt) 473 mL

    Principal Display Panel NDC 46122-331-43 ISOPROPYL RUBBING ALCOHOL 70% With Wintergreen Oil Rubbing, Massage, Sponge Bath 16 fl oz (1 pt) 473 mL

  • INGREDIENTS AND APPEARANCE
    GNP ISOPROPYL ALCOHOL 70 PERCENT WITH WINTERGREEN OIL 
    isopropyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:46122-331
    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
    METHYL SALICYLATE (UNII: LAV5U5022Y)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:46122-331-43473 mL in 1 BOTTLE; Type 0: Not a Combination Product01/01/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00301/01/2016
    Labeler - Amerisource Bergen (007914906)
    Registrant - Pharma Nobis, LLC (118564114)
    Establishment
    NameAddressID/FEIBusiness Operations
    Pharma Nobis, LLC118564114analysis(46122-331) , manufacture(46122-331) , pack(46122-331) , label(46122-331)
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