KLEENEX ANTIMICROBIAL SKIN CLEANSER (BENZALKONIUM CHLORIDE) SOLUTION [KIMBERLY-CLARK CORPORATION]

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  • KLEENEX ANTIMICROBIAL SKIN CLEANSER (BENZALKONIUM CHLORIDE) SOLUTION [KIMBERLY-CLARK CORPORATION]

KLEENEX ANTIMICROBIAL SKIN CLEANSER (BENZALKONIUM CHLORIDE) SOLUTION [KIMBERLY-CLARK CORPORATION]
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NDC 55118-440-10, 55118-440-12, 55118-440-15
Set ID 8453f826-9485-4239-9b76-ad50289a89c2
Category HUMAN OTC DRUG LABEL
Packager Kimberly-Clark Corporation
Generic Name
Product Class
Product Number
Application Number PART333E
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  • 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 TypeHUMAN OTC DRUGItem Code (Source)NDC:55118-440
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Benzalkonium Chloride (UNII: F5UM2KM3W7) (Benzalkonium - UNII:7N6JUD5X6Y) Benzalkonium Chloride0.013 mg  in 1 L
    Inactive Ingredients
    Ingredient NameStrength
    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 CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55118-440-101 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    2NDC:55118-440-121.2 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    3NDC:55118-440-151.5 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH NOT FINALpart333E06/20/2013
    Labeler - Kimberly-Clark Corporation (006072136)
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