Label: 70% ISOPROPYL ALCOHOL- isopropyl alcohol liquid

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

Drug Label Information

Updated January 30, 2025

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  • ACTIVE INGREDIENT

    Isopropyl Alcohol 70% v/v

  • INACTIVE INGREDIENT

    Water

  • PURPOSE

    First aid to help prevent the risk of infection in minor cuts, scrapes or burns.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

  • INDICATIONS & USAGE

    For the external use only

  • WARNINGS

    For external use only

    • If taken internally, serious gastric disturbances will result
    • flammable, keep away from heat or flame

    Ask a doctor before use if you have deep or puncture wounds, animal bites or serious burns

    When using this product

    • do not use in or near eyes. In case of contact with eyes, rinse eyes thoroughly with water
    • do not apply over large areas of the body
    • do not use longer than one week unless directed by a doctor

    Stop use and ask a doctor if irritation or rash appears

    Keep out of reach of children. In case of ingestion, get medical help or contact a Poison Control Center 1-800-222-1222 or dial 911 immediately

  • DOSAGE & ADMINISTRATION

    Clean affected area

    Apply small amount of this product on the affected area 1-3 times daily

    May be covered with a sterile bandage. If bandaged, let dry first

    children under 6 years of age should be supervised when using this product

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    70% ISOPROPYL ALCOHOL 
    isopropyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77039-010
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL70 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:77039-010-011000 mL in 1 BOTTLE; Type 0: Not a Combination Product01/12/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00501/12/2022
    Labeler - IDO PHARM (694853523)
    Registrant - IDO PHARM (694853523)
    Establishment
    NameAddressID/FEIBusiness Operations
    IDO PHARM694853523manufacture(77039-010)
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