Label: RUBBING ALCOHOL 99 PERCENT- isopropyl alcohol solution

  • NDC Code(s): 76436-318-16
  • Packager: Viny Health and Beauty Products Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 25, 2024

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  • Active ingredient

    ISOPROPYL ALCOHOL 99%

  • Purpose

    FIRST AID ANTISEPTIC

  • Uses

    FIRST AID TO HELP PREVENT THE RISK IN:

    • MINOR CUTS
    • SCRAPES BURNS
  • Keep Out of Reach of Children

    IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

    FOR RUBBING AND MASSAGING: CAUTION - DO NOT APPLY TO IRRITATED SKIN OR IF EXCESSIVE IRRITATION DEVELOPS. AVOID GETTING INTO THE EYES OR ON MUCOUS MEMBRANES.

  • WARNINGS

    For external use only.

    • FLAMMABLE, KEEP AWAY FROM FIRE OR FLAME, HEAT, SPARK, ELECTRICAL.
  • ASK DOCTOR

    ASK A DOCTOR BEFORE USE IF YOU HAVE

    • DEEP PUNCTURE WOUNDS SERIOUS BURNS
  • WHEN USING

    WHEN USING THIS PRODUCT

    • DO NOT GET INTO EYES
    • DO NOT APPLY OVER LARGE AREAS OF THE BODY.
    • DO NOT USE LONGER THAN 1 WEEK UNLESS DIRECTED BY A DOCTOR.
  • STOP USE

    STOP USE AND ASK A DOCTOR IF

    • CONDITION PERSISTS OR GET WORSE.
  • Directions

    • CLEAN THE AFFECTED AREA.
    • APPLY A SMALL AMOUNT OF THIS PRODUCT ON THE AREA 1 TO 3 TIMES DAILY
    • MAY BE COVERED WITH A STERILE BANDAGE
    • IF BANDAGED, LET DRY FIRST.
  • OTHER INFORMATION

    • 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

  • PRINCIPAL DISPLAY PANEL

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  • INGREDIENTS AND APPEARANCE
    RUBBING ALCOHOL 99 PERCENT 
    isopropyl alcohol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76436-318
    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:76436-318-16475 mL in 1 BOTTLE; Type 0: Not a Combination Product03/24/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00303/24/2024
    Labeler - Viny Health and Beauty Products Inc (079977276)
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