KLEENEX ANTIMICROBIAL SKIN CLEANSER- benzalkonium chloride solution 
Kimberly-Clark Corporation

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.

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KLEENEX® Antimicrobial Foam Skin Cleanser

Drug Facts

Active Ingredient

Benzalkonium Chloride 0.13%

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 to hands. 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/Eau/Aqua, Cocamidopropylamine Oxide, Polysilicone-20, Cetrimonium Chloride, Di-PPG-2 Myreth-10 Adipate, Benzyl Alcohol, Polymethacrylamidopropyltrimonium Chloride, Tetrasodium Iminodisuccinic Acid, Citric Acid, Aminomethyl Propanol

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 Bottle Label

Kleenex®
BRAND

Antimicrobial Foam
Skin Cleanser

Triclosan Free
1 Liter (33.8 fl oz)

20-14-736-0-00

Principal Display Panel - 1 Liter Bottle Label
KLEENEX ANTIMICROBIAL SKIN CLEANSER 
benzalkonium chloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55118-440
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Benzalkonium Chloride (UNII: F5UM2KM3W7) (Benzalkonium - UNII:7N6JUD5X6Y) Benzalkonium Chloride0.013 mg  in 1 L
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Cocamidopropylamine Oxide (UNII: M4SL82J7HK)  
Cetrimonium Chloride (UNII: UC9PE95IBP)  
Di-PPG-2 Myreth-10 Adipate (UNII: 4IN301M0KJ)  
Benzyl Alcohol (UNII: LKG8494WBH)  
Citric Acid Monohydrate (UNII: 2968PHW8QP)  
Aminomethylpropanol (UNII: LU49E6626Q)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55118-440-101 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
2NDC:55118-440-121.2 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
3NDC:55118-440-151.5 L 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 FINALpart333E06/20/2013
Labeler - Kimberly-Clark Corporation (006072136)

Revised: 11/2014
Document Id: a12a5460-496b-4d3e-ae66-8375f8a13a5f
Set id: 8453f826-9485-4239-9b76-ad50289a89c2
Version: 2
Effective Time: 20141112
 
Kimberly-Clark Corporation