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KLEENEX Antimicrobial Foam Skin Cleanser

Dosage form: solution
Ingredients: Benzalkonium Chloride 1mg in 1000mL
Labeler: Kimberly-Clark Corporation
NDC Code: 55118-700

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® Antimicrobial Foam Skin Cleanser

Drug Facts

Active Ingredient

Benzalkonium Chloride 0.1% w/w

Purpose

Antiseptic cleanser

Use

For personal hand hygiene to help prevent the spread of certain bacteria.

Warnings

For External Use Only. Do not ingest

Use with caution in children

When using this product avoid contact with eyes; in case of contact, flush eyes with water.

Discontinue use and consult a health care practitioner if irritation develops

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

Do not use if you are allergic to any ingredients.

Directions

Apply a small amount and lather hands in water for at least 30 seconds. Rinse well. Adults: Supervise children when using this product. Do not dilute product. For occasional use as needed.

Other Information

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

Inactive Ingredients

Aloe Barbadensis Leaf Juice Powder, Citric Acid, Coco-Betaine, Glycerin, Panthenol, Sodium Benzoate, Sodium Chloride, Sodium Hydroxide, Tocopheryl Acetate, Water.

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.

PRINCIPAL DISPLAY PANEL - 50.7 fl oz Bottle Label

Kleenex®
BRAND

Antimicrobial Foam
Skin Cleanser

Benzalkonium Chloride Solution, NF

new active ingredient
Benzalkonium
Chloride

DIN: 02443244
For Personal / Domestic Use Only

1.5 Liters (50.7 fl oz)

KLEENEX ANTIMICROBIAL FOAM SKIN CLEANSER 
benzalkonium chloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55118-700
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Benzalkonium Chloride (Benzalkonium) Benzalkonium Chloride1 mg  in 1000 mL
Inactive Ingredients
Ingredient NameStrength
Water 
Coco-Betaine 
Glycerin 
Sodium Chloride 
Sodium Benzoate 
Citric Acid Monohydrate 
Aloe 
Panthenol 
.Alpha.-Tocopherol Acetate 
Sodium Hydroxide 
Packaging
#Item CodePackage Description
1NDC:55118-700-18532 mL in 1 BOTTLE, PUMP
2NDC:55118-700-636 CARTRIDGE in 1 CARTON
2NDC:55118-700-101000 mL in 1 CARTRIDGE
3NDC:55118-700-652 CARTRIDGE in 1 CARTON
3NDC:55118-700-121200 mL in 1 CARTRIDGE
4NDC:55118-700-662 BOTTLE, DISPENSING in 1 CARTON
4NDC:55118-700-151500 mL in 1 BOTTLE, DISPENSING
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart333E09/01/2015
Labeler - Kimberly-Clark Corporation (006072136)

 
Kimberly-Clark Corporation

Medically reviewed on Sep 14, 2018

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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