KLEENEX HAND SANITIZER, GREEN CERTIFIED (ALCOHOL) SOLUTION [KIMBERLY-CLARK CORPORATION]

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KLEENEX HAND SANITIZER, GREEN CERTIFIED (ALCOHOL) SOLUTION [KIMBERLY-CLARK CORPORATION]
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NDC 55118-535-10, 55118-535-11, 55118-535-12, 55118-535-88, 55118-535-99
Set ID 590a1816-77e7-464f-b501-4d027becd6c3
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

    Ethyl Alcohol 70%

  • Purpose

    Antimicrobial

  • 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 immediately.

  • Directions

    Use enough foam to cover your hands. Rub hands together briskly until 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

    Aloe Barbadensis Leaf Extract, Betaine, Camellia Oleifera Leaf Extract, Citric Acid, Cucumis Sativus (Cucumber) Fruit Extract, Isopropanol, Glycerin, Meadowfoamamidopropyl Betaine, Panthenol, PEG-10 Dimethicone, Water

  • 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

    Foam
    Hand Sanitizer

    green
    certified

    CERTIFIED
    EcoLogo    ®
    Certified Instant
    Hand Antiseptic
    CCD-170

    8 fl oz (236 mL)

    20-14-611-0-00

    Principal Display Panel - 236 mL Bottle Label
  • INGREDIENTS AND APPEARANCE
    KLEENEX HAND SANITIZER, GREEN CERTIFIED 
    alcohol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55118-535
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M) Alcohol70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Isopropyl Alcohol (UNII: ND2M416302)  
    Betaine (UNII: 3SCV180C9W)  
    Citric Acid Monohydrate (UNII: 2968PHW8QP)  
    Panthenol (UNII: WV9CM0O67Z)  
    Glycerin (UNII: PDC6A3C0OX)  
    Aloe Vera Leaf (UNII: ZY81Z83H0X)  
    Camellia Oleifera Leaf (UNII: 5077EL0C60)  
    Cucumber (UNII: YY7C30VXJT)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55118-535-88236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    2NDC:55118-535-99473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    3NDC:55118-535-1145 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    4NDC:55118-535-101000 mL in 1 BAG; Type 0: Not a Combination Product
    5NDC:55118-535-121200 mL in 1 BAG; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH NOT FINALpart333E03/01/2012
    Labeler - Kimberly-Clark Corporation (006072136)
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