Label: KLEENEX HAND SANITIZER, GREEN CERTIFIED- alcohol solution

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

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 November 4, 2014

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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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