Label: KLEENEX REVEAL MOISTURIZING FOAM HAND SANITIZER- alcohol solution

  • NDC Code(s): 55118-531-10, 55118-531-11, 55118-531-12, 55118-531-18, view more
    55118-531-64, 55118-531-67
  • Packager: Kimberly-Clark
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 11, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Ethyl Alcohol 70% v/v

  • Purpose

    Antimicrobial

  • Uses

    For personal hand hygiene to help prevent the spread of bacteria. Kills harmful bacteria or germs.

  • Warnings

    For external use only

    Flammability warning

    Keep away from open flame and sources of heat.

    When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water.

    Stop use and 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 centre immediately.

  • Directions

    Use enough foam to cover your hands. Supervise children when they use this product. For occasional and personal domestic use. Rub thoroughly into hands for at least 30 seconds. Allow to dry. Use as part of your daily cleansing routine.

  • 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 Sensis Leaf Extract, Citric Acid, Cucumis Sativus Fruit Extract (Cucumber), Glycerin, Isopropanol, Meadowfoam Amidopropyl Betaine, Panthenol, PEG-10 Dimethicone, Water/Eau/Aqua

  • 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 - 532 mL Bottle Label

    Kleenex®
    BRAND
    MARQUE

    REVEAL™

    MOISTURIZING FOAM HAND SANITIZER

    ULTRA

    For Personal / Domestic Use Only
    18 fl oz (532 mL)

    PRINCIPAL DISPLAY PANEL - 532 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
    3NDC:55118-531-106 in 1 CARTON06/01/2022
    31000 mL in 1 BOTTLE; Type 0: Not a Combination Product
    4NDC:55118-531-122 in 1 CARTON06/01/2022
    41200 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph drugM00305/15/2018
    Labeler - Kimberly-Clark (830997032)
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