Label: 91% ISOPROPYL RUBBING ALCOHOL- isopropyl alcohol liquid

  • NDC Code(s): 51628-4236-1, 51628-4236-2, 51628-4236-3
  • Packager: MY IMPORTS USA LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 18, 2024

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

  • 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, etc.

    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 drug out of the reach of children

    • In case of an accidental ingestion, seek professional assistance or contact a Poison control center (1-800-222-1222) immediately

  • Directions

    • Clean effected 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

    Water(Aqua)

  • SPL UNCLASSIFIED SECTION

    AS 9175

    Use only in a well ventilated area

    Fumes may be harmful

    WARNING FLAMMABLE

    keep away from fire or flame!

    91% by volume

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

    Made in India

  • Packaging

    Label

  • INGREDIENTS AND APPEARANCE
    91% ISOPROPYL RUBBING ALCOHOL 
    isopropyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51628-4236
    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:51628-4236-1355 mL in 1 BOTTLE; Type 0: Not a Combination Product01/14/2021
    2NDC:51628-4236-2473 mL in 1 BOTTLE; Type 0: Not a Combination Product01/14/2021
    3NDC:51628-4236-3946 mL in 1 BOTTLE; Type 0: Not a Combination Product01/14/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00301/14/2021
    Labeler - MY IMPORTS USA LLC (195767988)
    Registrant - Jell Pharmaceuticals Pvt Ltd. (726025211)
    Establishment
    NameAddressID/FEIBusiness Operations
    Jell Pharmaceuticals Pvt Ltd.726025211manufacture(51628-4236)