Label: 70% ISOPROPYL RUBBING 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 70%

  • ASK DOCTOR

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

  • 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.

  • PURPOSE

    helps prevent the risk of infection in: minor cuts, scrapes, and 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

  • QUESTIONS

    Questions and Comments: www.bellechemical.com; 877-522-2233

  • DOSAGE & ADMINISTRATION

    • 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
  • WARNINGS

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

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

  • INACTIVE INGREDIENT

    Water

  • INDICATIONS & USAGE

    helps prevent the risk of infection in:

    • minor cuts
    • scrapes
    • burns
  • PRINCIPAL DISPLAY PANEL

    Label Image

  • INGREDIENTS AND APPEARANCE
    70% ISOPROPYL RUBBING ALCOHOL 
    70% isopropyl rubbing alcohol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82771-070
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL1 mL  in 700 mg
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82771-070-32700 mg in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/17/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)10/17/2022
    Labeler - Belle Chemical LLC (060891550)
    Registrant - Belle Chemical LLC (060891550)
    Establishment
    NameAddressID/FEIBusiness Operations
    Belle Chemical060891550manufacture(82771-070)
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