Label: UNIVERSAL RUBBING ALCOHOL- isopropyl alcohol liquid

  • NDC Code(s): 52000-406-35, 52000-406-36
  • Packager: Universal Distribution Center LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 12, 2024

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  • Drug Facts

  • Active ingredients (by volume):

    Isopropyl alcohol
    (91% 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 punctured 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 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 (1‑800‑222‑1222) immediately.

  • Directions

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

  • Other information

    • store at room temperature
    • 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

  • SPL UNCLASSIFIED SECTION

    For Rubbing and Massaging

    Use only in a well ventilated area; Fumes may be harmful.

    TAMPER EVIDENT: DO NOT USE IF THE UNDER CAP PRINTED SAFETY FOIL IS BROKEN OR MISSING.

    Made In Jordan

    Distributed by: Universal Distribution Center
    96 Distribution Boulevard • Edison, NJ 08817

  • Packaging

    rubbingalcohol406

  • INGREDIENTS AND APPEARANCE
    UNIVERSAL RUBBING ALCOHOL 
    isopropyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52000-406
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL91 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52000-406-35355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/01/2023
    2NDC:52000-406-36473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/01/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00306/01/2023
    Labeler - Universal Distribution Center LLC (019180459)
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