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
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated August 13, 2020

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

View All Sections
  • 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 not finalpart333A06/29/2012
    Labeler -  Universal Distribution Center LLC (019180459)
    Establishment
    NameAddressID/FEIBusiness Operations
    Anicare Pharmaceuticals Pvt. Ltd916837425manufacture(52000-001)
    Establishment
    NameAddressID/FEIBusiness Operations
    NOWREZ & ISMAIL SHUKRI COMPANY534665497manufacture(52000-001)
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!