Label: 99.9% ISOPROPYL ALCOHOL solution

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

Drug Label Information

Updated January 14, 2024

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  • ACTIVE INGREDIENT

    Isopropyl alcohol 99.9%

  • PURPOSE

    First Aid Antiseptic

  • WARNINGS

    For external use only. If taken internally serious gastric disturbances will result.

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

    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.

  • ASK DOCTOR

    Ask a doctor before use for deep or puncture wounds, animal bites or serious burns

  • WHEN USING

    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

    Stop use and ask doctor if condition persists or gets worse

  • 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.

  • DOSAGE & ADMINISTRATION

    Directions

    • clean the affected area
    • apply a small amount of this product on the area 1 to 3 times daily
    • may be covered with a sterile bandage
    • if bandaged, let dry first
  • INDICATIONS & USAGE

    helps prevent the risk of infection in:

    • minor cuts
    • scrapes
    • burns
  • SPL UNCLASSIFIED SECTION

    Other information:

    • does not contain, nor is intended as a substitute for grain or ethyl alcohol
  • INACTIVE INGREDIENT

    Water

  • QUESTIONS

    Questions and Comments:

    www.bellechemical.com

    877-522-2233

  • PRINCIPAL DISPLAY PANEL

    Label

  • INGREDIENTS AND APPEARANCE
    99.9% ISOPROPYL ALCOHOL 
    99.9% isopropyl alcohol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82771-999
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL999 mL  in 1000 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82771-999-32946 mL in 1 BOTTLE; Type 0: Not a Combination Product10/24/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)10/24/2022
    Labeler - Belle Chemical LLC (060891550)
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