Label: ISOPROPYL RUBBING ALCOHOL 99 PERCENT- isopropyl alcohol solution

  • NDC Code(s): 71611-402-12
  • Packager: MY Sales LLC dba Click Products LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 7, 2023

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  • Active ingredient

    ISOPROPYL ALCOHOL (99% CONC.)

  • Purpose

    FIRST AID ANTISEPTIC

  • Uses

    FIRST AID TO HELP PREVENT THE RISK IN:

    • MINOR CUTS
    • SCRAPES
    • BURNS
  • WARNINGS

    FOR EXTERNAL USE ONLY.

    • IF TAKEN INTERNALLY, SERIOUS GASTRIC DISTURBANCES WILL RESULT.

    FLAMMABLE, KEEP AWAY FROM FIRE OR FLAME

    • USE ONLY IN A WELL-VENTILATED AREA; FUMES MAY BE TOXIC.

    ASK A DOCTOR BEFORE USE IF YOU HAVE DEEP OR PUNCTURE WOUNDS, ANIMAL BITES, OR SERIOUS BURNS.

    WHEN USING THIS PRODUCT

    • DO NOT GET IN EYES
    • DO NOT APPLY OVER LARGE AREAS OF THE BODY
    • DO NOT USE LONGER THAN ONE WEEK UNLESS DIRECTED BY A DOCTOR

    STOP USE AND ASK A DOCTOR IF CONDITIONS PERSIST OR GET WORSE.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN. IN CASE OF INGESTION, GET MEDICAL HELP OR CONTACT A POSON CONTROL CENTER RIGHT AWAY.

  • Directions

    • CLEAN AFFECTED AREA
    • APPLY SMALL AMOUNT OF THIS PRODUCT ON THE AREA 1-3 TIMES DAILY
    • LET THE ALCOHOL DRY ON SKIN BEFORE USING BANDAGES
    • MAY BE COVERED WITH A STERILE BANDAGE

  • OTHER INFORMATION

    • STORE AT ROOM TEMPERATURE
    • DOES NOT CONTAIN, NOR IS INTENDED AS A SUBSTITUTE FOR GRAIN OR ETHYL ALCOHOL
  • Inactive Ingredient

    PURIFIED WATER

  • PRINCIPAL DISPLAY PANEL

    01b LBL_Wish_Rubbing Alcohol_99pct_Unscented_12oz

  • INGREDIENTS AND APPEARANCE
    ISOPROPYL RUBBING ALCOHOL  99 PERCENT
    isopropyl alcohol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71611-402
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL99 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71611-402-12355 mL in 1 BOTTLE; Type 0: Not a Combination Product11/25/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00311/25/2020
    Labeler - MY Sales LLC dba Click Products LLC (080766174)
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