KLEENEX ANTISEPTIC HAND RUB WITH MOISTURIZERS (ALCOHOL) SOLUTION [KIMBERLY-CLARK CORPORATION]

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  • KLEENEX ANTISEPTIC HAND RUB WITH MOISTURIZERS (ALCOHOL) SOLUTION [KIMBERLY-CLARK CORPORATION]

KLEENEX ANTISEPTIC HAND RUB WITH MOISTURIZERS (ALCOHOL) SOLUTION [KIMBERLY-CLARK CORPORATION]
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NDC 55118-580-10
Set ID a9ea5b54-509e-48e0-a5e5-f5f5428feb84
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% v/v

  • Purpose

    Antiseptic

  • 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 or persists.

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

  • 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, Aminomethyl Propanol, Carbomer, Ceteth-10, Dimethicone, Glycerin, Hydroxypropylcellulose, Isopropanol, Panthenol, Petrolatum, Poloxamer 335, Steareth-21, Tocopheryl Acetate, 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 - 1 Liter Container Label

    Kleenex®
    BRAND

    Antiseptic Hand Rub
    with Moisturizers

    hydrates
    skin

    1 Liter (33.8 fl oz)

    20-14-695-0-00

    PRINCIPAL DISPLAY PANEL - 1 Liter Container Label
  • INGREDIENTS AND APPEARANCE
    KLEENEX ANTISEPTIC HAND RUB WITH MOISTURIZERS 
    alcohol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55118-580
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M) Alcohol0.7 L  in 1 L
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Glycerin (UNII: PDC6A3C0OX)  
    Dimethicone (UNII: 92RU3N3Y1O)  
    Liquid Petroleum (UNII: 6ZAE7X688J)  
    Aminomethylpropanol (UNII: LU49E6626Q)  
    Hydroxypropyl Cellulose (Type H) (UNII: RFW2ET671P)  
    Ceteth-10 (UNII: LF9X1PN3XJ)  
    Steareth-21 (UNII: 53J3F32P58)  
    Aloe Vera Leaf (UNII: ZY81Z83H0X)  
    Panthenol (UNII: WV9CM0O67Z)  
    Poloxamer 335 (UNII: G6DQL26D50)  
    .Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55118-580-101 L in 1 CONTAINER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH NOT FINALpart333E05/15/2012
    Labeler - Kimberly-Clark Corporation (006072136)
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