Label: KLEENEX INSTANT HAND SANITIZER- alcohol solution

  • NDC Code(s): 55118-704-70, 55118-704-88
  • Packager: Kimberly-Clark Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 10, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient

    Ethyl Alcohol 68% v/v

  • Purpose

    Antiseptic

  • Use

    Hand sanitizer to decrease bacteria on the skin.

  • Warnings

    Flammable - Keep product away from fire or flame.

    For External Use Only.

    When using this product avoid contact with eyes; in case of contact, flush eyes with water.

    Stop use & ask a doctor if irritation or redness develops and persists.

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    Wet hands thoroughly with product and allow to dry.

  • Other Information

    • Report serious side effects from this product to 1-877-561-6587.
    • Do not store above 110°F (40°C).
  • Inactive Ingredients

    Water, Carbomer, Fragrance, Aminomethyl Propanol, Glycerin

  • Questions?

    1-888-346-4652

  • SPL UNCLASSIFIED SECTION

    Distributed in the U.S. by
    Kimberly-Clark
    Global Sales, LLC, Roswell,
    GA 30076-2199

  • PRINCIPAL DISPLAY PANEL - 236 mL Bottle Label

    Kleenex®
    BRAND
    MARQUE

    Instant Hand
    Sanitizer

    kills
    germs†

    8 fl oz (236 mL)

    20-14-141-0-09

    PRINCIPAL DISPLAY PANEL - 236 mL Bottle Label
  • INGREDIENTS AND APPEARANCE
    KLEENEX INSTANT HAND SANITIZER 
    alcohol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55118-704
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M) Alcohol68 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55118-704-706 in 1 CARTON08/30/2021
    1NDC:55118-704-88236 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph drugM00308/30/2021
    Labeler - Kimberly-Clark Corporation (830997032)
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