Label: ISOPROPYL ALCOHOL liquid

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

Drug Label Information

Updated November 5, 2023

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  • Active Ingredient

    Isopropyl alcohol 91%

    Purpose

    First Aid Antiseptic

  • Inactive Ingredients

    Water

  • Uses

    First aid to help prevent the risk of infection in:

    • Minor cuts
    • Scrapes
    • Burns
  • Warnings

    For external use onlyFlammable

    • Keep away from fire or flame, heat, spark, electrical

    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 inhale
    • Do not apply over large areas of the body
    • Do not use longer than 1 week

    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.

    Caution

    Fumes can be acutely irritating to skin, eyes and the respiratory system. Do not apply to irritated skin or if excessive irritation develops. Avoid getting into the eyes or on mucous membranes. Avoid inhaling this product.

  • Directions

    • Clean the affected area.
    • Apply a small amount of product on the area 1 o 3 times daily
    • May be covered with a sterile bandage.
    • If bandaged, let dry first.
  • Other Information

    • Does not contain, nor is intended as a substitute for grain or ethyl alcohol
    • Will produce serious gastric disturbances if taken internally
  • Question or comments?

    Call 956 728-8899

  • Package Labeling:

    Bottle

  • INGREDIENTS AND APPEARANCE
    ISOPROPYL ALCOHOL 
    isopropyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67326-035
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL0.91 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67326-035-00473 mL in 1 BOTTLE; Type 0: Not a Combination Product10/20/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)10/20/2020
    Labeler - Degasa, S.A. de C.V. (812771980)
    Establishment
    NameAddressID/FEIBusiness Operations
    Degasa, S.A. de C.V.812771980manufacture(67326-035)
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