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KLEENEX Foam Hand Sanitizer

Medically reviewed by Drugs.com. Last updated on Oct 8, 2021.

Dosage form: solution
Ingredients: Benzalkonium Chloride 1.3mg in 1000mL
Labeler: Kimberly-Clark
NDC Code: 55118-701

KLEENEX® Foam Hand Sanitizer

Drug Facts

Active Ingredient

Benzalkonium Chloride 0.13% 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 small amount and rub thoroughly into hands for at least 30 seconds. Allow to dry. Not to be rinsed off with water (i.e. not to be used as a handwash ). For occasional use as needed. Adults: Supervise children when using this product.

Other Information

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

Inactive Ingredients

Aloe Barbadensis Leaf Juice Powder, Calcium, Citric Acid, Cocamidopropyl PG-Dimonium Chloride Phosphate, Methylpropanediol, Panthenol, PEG-14M, Silica, Sodium Hydroxide, 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 - 473 mL Bottle Label

Kleenex®
BRAND

Foam Hand Sanitizer

Benzalkonium Chloride Solution, NF

alcohol
free

DIN: 02443252

For Personal /
Domestic Use Only

16 fl oz (473 mL)

20-14-637-0-02

KLEENEX FOAM HAND SANITIZER 
benzalkonium chloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55118-701
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Benzalkonium Chloride (Benzalkonium) Benzalkonium Chloride1.3 mg  in 1000 mL
Inactive Ingredients
Ingredient NameStrength
Water 
Methylpropanediol 
Cocamidopropyl Propylene Glycol-Dimonium Chloride Phosphate 
Polyethylene Oxide 600000 
Citric Acid Monohydrate 
Silicon Dioxide 
Aloe 
Panthenol 
Calcium 
Sodium Hydroxide 
Packaging
#Item CodePackage Description
1NDC:55118-701-6424 BOTTLE, PUMP in 1 CARTON
1NDC:55118-701-1145 mL in 1 BOTTLE, PUMP
2NDC:55118-701-99473 mL in 1 BOTTLE, PUMP
3NDC:55118-701-101000 mL in 1 CARTRIDGE
4NDC:55118-701-121200 mL in 1 CARTRIDGE
5NDC:55118-701-674 BOTTLE, PUMP in 1 CARTON
5NDC:55118-701-18532 mL in 1 BOTTLE, PUMP
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart333E09/01/2015
Labeler - Kimberly-Clark (830997032)

 
Kimberly-Clark

Further information

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