Label: AMERICAN RED CROSS 50 ISOPROPYL RUBBING ALCOHOL- isopropyl alcohol liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated February 13, 2022

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  • Drug Facts

  • Active ingredient

    Isopropyl alcohol (50% conc.)

    Purpose

    First aid antiseptic

  • Uses

    • first aid to help prevent the risk of infection in minor cuts, scrapes and burns 
    • helps relieve minor muscular aches due to exertion
  • Warnings

    For external use only.

    Flammable, keep away from heat, spark, electrical, fire or flame

    • will produce serious gastric disturbances if taken internally

    Do not use

    • in the eyes or apply over large areas of the body 
    • longer than 1 week 
    • do not inhale

    Ask a doctor before use if you have

    deep or punture wounds, animal bites or serious burns.

    Stop use and ask a doctor if

    • the condition persists or gets worse 
    • irritation, pain, or redness persists or worsens
    • swelling, rash, or fever develops

    Kepp out of reach of children.

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

  • Directions

    • clean the affected area
    • apply a small amount of product on the affected area 1 to 3 times a day
    • may be covered with a sterile bandage
    • if bandaged, let dry first
  • Other information 

    • keep tightly closed and at controlled room temperature
    • does not contain, nor is intended as a substitute for grain or ethyl alcohol
  • Inactive ingredients

    purified water

  • Package Labeling:

    Label

  • INGREDIENTS AND APPEARANCE
    AMERICAN RED CROSS 50 ISOPROPYL RUBBING ALCOHOL 
    isopropyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51628-4432
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL500 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:51628-4432-0177 mL in 1 BOTTLE; Type 0: Not a Combination Product03/10/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A03/10/2022
    Labeler - MY IMPORTS USA LLC (195767988)
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