Label: ISOPROPYL RUBBING ALCOHOL- isopropyl alcohol solution

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

Drug Label Information

Updated November 3, 2023

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient

    Isopropyl Alcohol 70% v/v

  • 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 havedeep 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

    • the 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 infected 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

  • PRINCIPAL DISPLAY PANEL 

    Rubbing Alcohol

    70% Isopropyl

    first aid antiseptic

    Tamper evident cap for your protection.
    If ring-band is detached from cap or missing do not use.

    WARNING:Flammable

    4 FL. OZ. (118 mL)

    PRINCIPAL DISPLAY PANEL

  • INGREDIENTS AND APPEARANCE
    ISOPROPYL RUBBING ALCOHOL 
    isopropyl alcohol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10202-002
    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:10202-002-04118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/03/2011
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)02/03/2011
    Labeler - 7-Eleven, Inc. (007347602)
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