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KLEENEX Antibacterial Clear Skin Cleanser

Dosage form: solution
Ingredients: Triclosan 2.5g in 1L
Labeler: Kimberly-Clark Corporation
NDC Code: 55118-200

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.

MARQUE
kleenex®
BRAND
ANTIBACTERIAL Clear SKIN CLEANSER

Drug Facts

Active Ingredient

Triclosan Liquid 0.25% w/w

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 and persists.

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

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

Ingredients

Water, Sodium Laureth Sulfate, Sodium Chloride, Cocamidopropyl Betaine, Cocamide DEA, Glycerin, Propylene Glycol, Fragrance, Panthenol, Aloe Barbadensis Leaf Juice, Citric Acid, Methylchloroisothiazolinone, Methylisothiazolinone

Questions?

1-888-346-4652

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

www.kcprofessional.com

PRINCIPAL DISPLAY PANEL - 1 Liter Bottle Label

Kimberly-Clark
PROFESSIONAL*

MARQUE
kleenex®
BRAND

ANTIBACTERIAL Clear SKIN CLEANSER

Triclosan Liquid 0.25%

1 Liter (33.8 fl oz)

DIN: 02243381
NDC: 055118-200-10

20-14-472-0-02

KLEENEX ANTIBACTERIAL CLEAR SKIN CLEANSER 
triclosan solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55118-200
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Triclosan (Triclosan) Triclosan2.5 g  in 1 L
Inactive Ingredients
Ingredient NameStrength
Water 
Sodium Laureth Sulfate 
Sodium Chloride 
Cocamidopropyl Betaine 
Coco Diethanolamide 
Glycerin 
Propylene Glycol 
Panthenol 
Aloe Vera Leaf 
Citric Acid Monohydrate 
Methylchloroisothiazolinone 
Methylisothiazolinone 
Packaging
#Item CodePackage Description
1NDC:55118-200-101 L in 1 CARTRIDGE
2NDC:55118-200-050.5 L in 1 BOTTLE, PLASTIC
3NDC:55118-200-080.8 L in 1 BOTTLE, PLASTIC
4NDC:55118-200-151.5 L in 1 CARTRIDGE
5NDC:55118-200-252.5 L in 1 CARTRIDGE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart333E03/01/2011
Labeler - Kimberly-Clark Corporation (006072136)

Revised: 04/2011
Document Id: e2b1a0d0-97f3-4f5f-b91a-c4487f69c976
Set id: 7ce348ea-50b0-4c35-b090-6d912055cf35
Version: 1
Effective Time: 20110415
 
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 drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.

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