Label: MEDICHOICE ISOPROPYL RUBBING ALCOHOL- isopropyl alcohol liquid

  • NDC Code(s): 39892-0500-1, 39892-0500-2
  • Packager: Owens & Minor Distribution, Inc.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated November 14, 2024

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  • Drug Facts

  • Active ingredient

    Isopropyl alcohol 70%

    Purpose

    First Aid Antiseptic

  • Uses

    • first aid to help prevent the risk of infection in: • minor cuts • scrapes • burns

  • Warnings

    For external use only

    Flammable• keep away from fire or flame, heat, spark, electrical. Flash point 72°F.
    • do not use with electrocautery procedures.

    Ask a doctor before use if you have

    deep or puncture wounds, animal bites or 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 unless directed by a doctor

    Stop use and ask a doctor if

    condition persists or gets worse

    Keep out of reach of children. 

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • clean the affected area • apply 1 to 3 times daily

  • Other information

    • does not contain, nor is intended as a substitute for grain or ethyl alcohol • will produce serious gastric disturbances if taken internally

  • Inactive ingredient

    purified water

  • MediChoice Isopropyl Rubbing Alcohol, USP 4 FI.Oz./118mL (39892-0500-1)

    Label4

  • MediChoice Isopropyl Rubbing Alcohol, USP 16 FI.Oz./473mL (39892-0500-2)

    Label5

  • INGREDIENTS AND APPEARANCE
    MEDICHOICE ISOPROPYL RUBBING ALCOHOL 
    isopropyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:39892-0500
    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:39892-0500-1118 mL in 1 BOTTLE; Type 0: Not a Combination Product03/20/2019
    2NDC:39892-0500-2473 mL in 1 BOTTLE; Type 0: Not a Combination Product03/20/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00303/20/2019
    Labeler - Owens & Minor Distribution, Inc. (847412269)
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