Label: ALCOHOL- isopropyl alcohol spray

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

Drug Label Information

Updated January 24, 2024

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  • ACTIVE INGREDIENT

    Active Ingredient:

    Isopropyl Alcohol 70%

  • PURPOSE

    Purpose:

    First aid antiseptic

  • INDICATIONS & USAGE

    Uses:

    First aid to help prevent infection in minor cuts, scrapes, and burns

  • WARNINGS

    Warnings

    For external use only

    Flammable, keep away from fire or flames

  • DO NOT USE

    Do not use

    • in the eyes
    • over large portions of the body
    • on deep or puncture wounds
    • on animal bites
    • on serious burns
  • STOP USE

    Stop use and ask a doctor if

    • the condition worsens
    • the condition lasts for more than 7 days
  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away. 1-800-222-1222

  • DOSAGE & ADMINISTRATION

    Directions:

    Adults and children 2 years of age and over: apply topically to clean the affected area not more than 3 times daly

    Children under 2 years of age: ask a doctor

  • INACTIVE INGREDIENT

    Inactive ingredient

    Purified Water

  • PRINCIPAL DISPLAY PANEL

    2711Alcoholv20f.jpg

  • INGREDIENTS AND APPEARANCE
    ALCOHOL 
    isopropyl alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50332-0213
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50332-0213-160 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product05/04/2012
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM05/04/2012
    Labeler - NorMed (069560969)