Label: KLEENEX E2 FOAM SKIN CLEANSER- chloroxylenol 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 May 10, 2012

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient

    Chloroxylenol 1.75%

  • Purpose

    Antiseptic

  • Use

    For handwashing to decrease bacteria on the skin.

  • Warnings

    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

    Wet hands and apply a palmful. Scrub thoroughly for 15-20 seconds. Rinse and dry thoroughly.

  • Other Information

    Report serious side effects from this product to 1-877-561 -6587

  • Inactive Ingredients

    Water, Hexylene Glycol, Sodium Laureth Sulfate, Cocamidopropyl Betaine, Disodium EDTA, Sodium Hydroxide, MethylchloroisothiazoIinone, Methylisothiazolinone

  • 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

    E-2 Foam
    Skin Cleanser

    1 Liter (33.8 fl oz)

    20-14-464-0-04

    PRINCIPAL DISPLAY PANEL - 1 Liter Container Label
  • INGREDIENTS AND APPEARANCE
    KLEENEX E2 FOAM SKIN CLEANSER 
    chloroxylenol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55118-570
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Chloroxylenol (UNII: 0F32U78V2Q) (Chloroxylenol - UNII:0F32U78V2Q) Chloroxylenol0.0175 L  in 1 L
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Hexylene Glycol (UNII: KEH0A3F75J)  
    Sodium Laureth Sulfate (UNII: BPV390UAP0)  
    Cocamidopropyl Betaine (UNII: 5OCF3O11KX)  
    Edetate Disodium (UNII: 7FLD91C86K)  
    Sodium Hydroxide (UNII: 55X04QC32I)  
    Methylchloroisothiazolinone (UNII: DEL7T5QRPN)  
    Methylisothiazolinone (UNII: 229D0E1QFA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55118-570-101 L in 1 CONTAINER
    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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