Label: KLEENEX HAND SANITIZER- 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 3, 2014

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  • Drug Facts

  • Active Ingredient

    Ethyl Alcohol, 70%

  • 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 & consult a health care practitioner if irritation or redness develops or persists.

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

  • Directions

    Wet hands thoroughly with product. Rub hands together briskly until dry.

  • Other Information

    Report serious side effects from this product to 1-877-561-6587 Do not store above 37.8 C / 100 F

  • Inactive Ingredients

    Carbopol 1342, Glycerol, Orange Flower Oil, Propylene Glycol, Triethanolamine, Water

  • Questions?

    1-888-346-4652

  • PRINCIPAL DISPLAY PANEL - 50 mL Bottle Label

    Kleenex ® BRAND

    Hand Sanitizer Gel

    Kills 99.9% of germs

    1.7 fl oz / 50 mL

    Principal Display Panel - 50 mL Bottle Label
  • INGREDIENTS AND APPEARANCE
    KLEENEX HAND SANITIZER 
    alcohol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55118-610
    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
    Carbomer Copolymer Type B (Allyl Pentaerythritol Crosslinked) (UNII: 809Y72KV36)  
    Glycerin (UNII: PDC6A3C0OX)  
    Citrus Sinensis Flower Oil (UNII: AJ56JP5TFP)  
    Propylene Glycol (UNII: 6DC9Q167V3)  
    Trolamine (UNII: 9O3K93S3TK)  
    Water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55118-610-5050 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH NOT FINALpart333E09/01/2013
    Labeler - Kimberly-Clark Corporation (006072136)
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