KLEENEX E2 Foam Skin Cleanser

Dosage form: solution
Ingredients: Chloroxylenol 0.0175L in 1L
Labeler: Kimberly-Clark Corporation
NDC Code: 55118-570

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.

KLEENEX® E2 Foam Skin Cleanser

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

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

KLEENEX E2 FOAM SKIN CLEANSER 
chloroxylenol solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55118-570
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Chloroxylenol (Chloroxylenol) Chloroxylenol0.0175 L  in 1 L
Inactive Ingredients
Ingredient NameStrength
Water 
Hexylene Glycol 
Sodium Laureth Sulfate 
Cocamidopropyl Betaine 
Edetate Disodium 
Sodium Hydroxide 
Methylchloroisothiazolinone 
Methylisothiazolinone 
Packaging
#Item CodePackage Description
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)

Revised: 05/2012
 
Kimberly-Clark Corporation

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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