KLEENEX ANTIMICROBIAL SKIN CLEANSER- benzalkonium chloride solution

KLEENEX Antimicrobial Skin Cleanser by

Drug Labeling and Warnings

KLEENEX Antimicrobial Skin Cleanser by is a Otc medication manufactured, distributed, or labeled by Kimberly-Clark Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

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

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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

INGREDIENTS AND APPEARANCE

KLEENEX ANTIMICROBIAL SKIN CLEANSER 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55118-440
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Benzalkonium Chloride (UNII: F5UM2KM3W7) (Benzalkonium - UNII:7N6JUD5X6Y)	Benzalkonium Chloride	0.013 mg  in 1 L

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55118-440-10	1 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
2	NDC: 55118-440-12	1.2 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
3	NDC: 55118-440-15	1.5 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part333E	06/20/2013

Labeler - Kimberly-Clark Corporation (006072136)