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KLEENEX Antibacterial Foam Skin Cleanser (Kimberly-Clark Corporation)

Available Formats

Dosage Form Package Information Links
SOLUTION 1 L in 1 CONTAINER (55118-565-10) Label Information

Complete KLEENEX Antibacterial Foam Skin Cleanser Information

  • SPL UNCLASSIFIED SECTION

    Drug Facts


  • Active Ingredient

    Triclosan, 0.50% w/w


  • Purpose

    Antiseptic


  • Use

    Antiseptic cleanser. For personal hand hygiene to help prevent the spead of certain bacteria.


  • 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 health care practitioner if irritation or redness develops or persists.

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


  • Directions

    Wet hands and apply a palmful to hands. Scrub thoroughly for 15-20 seconds. Rinse and dry thoroughly. Use as part of your daily cleansing routine.


  • Other Information

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


  • Inactive Ingredients

    Water/Eau, Propylene Glycol, Sodium Citrate, Sodium Cumenesulfonate, Sodium Laureth Sulfate, Citric Acid, Cocamidopropyl Betaine, PEG-7 Glyceryl Cocoate, Fragrance/Parfum, Disodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone.


  • Questions?

    1-888-346-4652


  • SPL UNCLASSIFIED SECTION

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

    Distributed in Canada by Kimberly-Clark Inc., Mississauga, Ontario L5B 3Y5


  • PRINCIPAL DISPLAY PANEL - 1.2 Liter Container Label

    MARQUE
    Kleenex®
    BRAND

    Antibacterial Foam Skin Cleanser

    Triclosan Solution, House Std., 0.50%

    DIN:02339641
    For Personal / Domestic Use Only

    1.2 Liters (40.5 fl oz)

    20-14-700-0-00

    Principal Display Panel - 1.2 Liter Container Label

  • INGREDIENTS AND APPEARANCE
    KLEENEX ANTIBACTERIAL SKIN CLEANSER 
    triclosan solution
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:55118-565
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Triclosan (UNII: 4NM5039Y5X) (Triclosan - UNII:4NM5039Y5X) Triclosan 5 g  in 1 L
    Inactive Ingredients
    Ingredient Name Strength
    water (UNII: 059QF0KO0R)  
    Propylene Glycol (UNII: 6DC9Q167V3)  
    Sodium Citrate (UNII: 1Q73Q2JULR)  
    Sodium Cumenesulfonate (UNII: 5798KA13PG)  
    Sodium Laureth-3 Sulfate (UNII: BPV390UAP0)  
    Citric Acid Monohydrate (UNII: 2968PHW8QP)  
    Cocamidopropyl Betaine (UNII: 5OCF3O11KX)  
    PEG-7 Glyceryl Cocoate (UNII: VNX7251543)  
    Edetate Disodium (UNII: 7FLD91C86K)  
    Methylchloroisothiazolinone (UNII: DEL7T5QRPN)  
    Methylisothiazolinone (UNII: 229D0E1QFA)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:55118-565-10 1 L in 1 CONTAINER; Type 0: Not a Combination Product
    2 NDC:55118-565-12 1.2 L in 1 CONTAINER; Type 0: Not a Combination Product
    3 NDC:55118-565-15 1.5 L in 1 CONTAINER; 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 05/15/2012
    Labeler - Kimberly-Clark Corporation (006072136)
    Establishment
    Name Address ID/FEI Business Operations
    Marietta Corporation 010765394 MANUFACTURE(55118-565) , ANALYSIS(55118-565) , RELABEL(55118-565)