Label: UNIVERSAL 50% RUBBING ALCOHOL- isopropyl alcohol liquid

  • NDC Code(s): 52000-410-32
  • Packager: Universal Distribution Center LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 22, 2024

If you are a consumer or patient please visit this version.

View All Sections
  • Drug Facts

  • Active ingredients (by volume):

    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 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 & 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

    50%IPA

  • INGREDIENTS AND APPEARANCE
    UNIVERSAL 50% RUBBING ALCOHOL 
    isopropyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52000-410
    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:52000-410-32946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/01/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00307/01/2023
    Labeler - Universal Distribution Center LLC (019180459)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!