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KLEENEX Antimicrobial Foam Skin Cleanser (Kimberly-Clark Corporation)

Available Formats

Dosage Form Package Information Links
SOLUTION 1.2 L in 1 BOTTLE, PLASTIC (55118-440-12) Label Information
SOLUTION 1.5 L in 1 BOTTLE, PLASTIC (55118-440-15) Label Information
SOLUTION 1 L in 1 BOTTLE, PLASTIC (55118-440-10) Label Information

Complete KLEENEX Antimicrobial Foam Skin Cleanser Information

  • SPL UNCLASSIFIED SECTION

    Drug Facts


  • Active Ingredient

    Benzalkonium Chloride 0.13%


  • Purpose

    Antiseptic


  • Use

    For handwashing to decrease bacteria on the skin.


  • Warnings

    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 or persists.

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


  • Directions

    Wet hands and apply a palmful to hands. Scrub thoroughly for 15-20 seconds. Rinse and dry thoroughly.


  • Other Information

    Report serious side effects from this product to 1-877-561-6587


  • Inactive Ingredients

    Water/Eau/Aqua, Cocamidopropylamine Oxide, Polysilicone-20, Cetrimonium Chloride, Di-PPG-2 Myreth-10 Adipate, Benzyl Alcohol, Polymethacrylamidopropyltrimonium Chloride, Tetrasodium Iminodisuccinic Acid, Citric Acid, Aminomethyl Propanol


  • 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 - 1 Liter Bottle Label

    Kleenex®
    BRAND

    Antimicrobial Foam
    Skin Cleanser

    Triclosan Free
    1 Liter (33.8 fl oz)

    20-14-736-0-00

    Principal Display Panel - 1 Liter Bottle Label

  • INGREDIENTS AND APPEARANCE
    KLEENEX ANTIMICROBIAL SKIN CLEANSER 
    benzalkonium chloride solution
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:55118-440
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Benzalkonium Chloride (UNII: F5UM2KM3W7) (Benzalkonium - UNII:7N6JUD5X6Y) Benzalkonium Chloride 0.013 mg  in 1 L
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    Cocamidopropylamine Oxide (UNII: M4SL82J7HK)  
    Cetrimonium Chloride (UNII: UC9PE95IBP)  
    Di-PPG-2 Myreth-10 Adipate (UNII: 4IN301M0KJ)  
    Benzyl Alcohol (UNII: LKG8494WBH)  
    Citric Acid Monohydrate (UNII: 2968PHW8QP)  
    Aminomethylpropanol (UNII: LU49E6626Q)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:55118-440-10 1 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    2 NDC:55118-440-12 1.2 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    3 NDC:55118-440-15 1.5 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC MONOGRAPH NOT FINAL part333E 06/20/2013
    Labeler - Kimberly-Clark Corporation (006072136)