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

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 July 13, 2023

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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 not finalpart333E08/30/2021
    Labeler - Kimberly-Clark Corporation (830997032)
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