KLEENEX REVEAL MOISTURIZING FOAM HAND SANITIZER (ALCOHOL) SOLUTION [KIMBERLY-CLARK CORPORATION]

KLEENEX REVEAL MOISTURIZING FOAM HAND SANITIZER (ALCOHOL) SOLUTION [KIMBERLY-CLARK CORPORATION]
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NDC 55118-531-11, 55118-531-18, 55118-531-64, 55118-531-67
Set ID 4a491f90-268e-470d-a74c-473f1efe7c8b
Category HUMAN OTC DRUG LABEL
Packager Kimberly-Clark
Generic Name
Product Class
Product Number
Application Number PART333E
  • 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, Camellis Sinensis Leaf Extract, Citric Acid, Cucumis Sativus (Cucumber) Fruit Extract, Isooropanol, 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. Distributed
    in Canada by Kimberly-Clark Inc., Mississauga, Ontario L5B 3Y5.

  • PRINCIPAL DISPLAY PANEL - 45 mL Bottle Label

    Kleenex® BRAND

    REVEAL™
    MOISTURIZING FOAM
    HAND SANITIZER

    ULTRA

    NPN: 80030706

    For Personal / Domestic Use Only

    1.5 fl oz (45 mL)

    Principal Display Panel - 45 mL Bottle Label
  • INGREDIENTS AND APPEARANCE
    KLEENEX REVEAL MOISTURIZING FOAM HAND SANITIZER 
    alcohol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55118-531
    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
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Betaine (UNII: 3SCV180C9W)  
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    CUCUMBER (UNII: YY7C30VXJT)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    Glycerin (UNII: PDC6A3C0OX)  
    Meadowfoamamidopropyl Betaine (UNII: HNV0L650LG)  
    Panthenol (UNII: WV9CM0O67Z)  
    PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)  
    Water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55118-531-6424 in 1 CARTON05/15/2018
    1NDC:55118-531-1145 mL in 1 BOTTLE; Type 0: Not a Combination Product
    2NDC:55118-531-674 in 1 CARTON05/15/2018
    2NDC:55118-531-18532 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E05/15/2018
    Labeler - Kimberly-Clark (830997032)

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