Label: ALLURE ISOPROPYL RUBBING ALCOHOL- isopropyl alcohol liquid

  • NDC Code(s): 52000-001-01, 52000-001-02, 52000-001-03, 52000-001-04, view more
    52000-001-05, 52000-001-06, 52000-001-07
  • Packager: Universal Distribution Center LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 12, 2024

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  • Active Ingredients

    Isopropyl alcohol (50% conc.)

  • Purpose

    First aid antiseptic

  • Uses

    First aid to help prevent the risk of infection in minor cuts, scrapes and burns

  • Warnings

    For external use only

    • flammable, keep away from fire or flame, heat, spark, electrical
  • Ask a doctor before use if you have

    • deep puncture wounds, animal bites or serious burns
  • When using this product

    • do not get into eyes
    • do not apply over large areas of body
    • do not use longer than one week unless directed by a doctor
  • Stop using this product if

    • condition persists or gets worse
  • Keep this and all drugs out of the reach of children

    In case of accidental ingestion, seek professional assistance or contact a Poison control center (1-800-222-1212) immediately

  • Directions

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

  • Inactive ingredient

    purified water

  • Packaging

    untitled

  • INGREDIENTS AND APPEARANCE
    ALLURE ISOPROPYL RUBBING ALCOHOL 
    isopropyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52000-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL50 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52000-001-01118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/29/2012
    2NDC:52000-001-02177 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/29/2012
    3NDC:52000-001-03237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/29/2012
    4NDC:52000-001-04296 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/29/2012
    5NDC:52000-001-05355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/29/2012
    6NDC:52000-001-06414 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/29/2012
    7NDC:52000-001-07473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/29/2012
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00306/29/2012
    Labeler -  Universal Distribution Center LLC (019180459)
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