DrugCite

KLEENEX ALCOHOL FREE FOAM HAND SANITIZER - benzalkonium chloride solution 
Kimberly-Clark Corporation

KLEENEX® Alcohol Free Foam Hand Sanitizer

Drug Facts

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antimicrobial

Use

Hand sanitizer 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

Use enough foam to cover your hands. Rub hands together briskly until dry.

Other Information

  • Report serious side effects from this product to 1-877-561-6587
  • Do not store above 110° F (40° C).

Inactive Ingredients

Allantoin, Cetrimonium Chloride, Cocamidopropyl Betaine, Cocamidopropylamine Oxide, Diazolidinyl Urea, Didecyldimonium Chloride, Methylparaben, Propylene Glycol, Propylparaben, Triethanolamine, Water.

Questions?

1-888-346-4652

Distributed in the U.S. by Kimberly-Clark Global
Sales, LLC, Roswell, GA 30076-2199

PRINCIPAL DISPLAY PANEL - 45 mL Bottle Label

Kleenex®
BRAND

Foam Hand
Sanitizer

alcohol
free

1.5 fl oz (45 mL)

Principal Display Panel - 45 mL Bottle Label

KLEENEX ALCOHOL FREE FOAM HAND SANITIZER 
benzalkonium chloride  solution
Product Information
Product Type HUMAN OTC DRUG NDC Product Code (Source) 55118-541
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Benzalkonium Chloride (Benzalkonium) Benzalkonium Chloride 1.3 mg  in 1 mL
Inactive Ingredients
Ingredient Name Strength
WATER  
ALLANTOIN  
CETRIMONIUM CHLORIDE  
COCAMIDOPROPYL BETAINE  
COCAMIDOPROPYLAMINE OXIDE  
DIDECYLDIMETHYLAMMONIUM CHLORIDE  
PROPYLPARABEN  
PROPYLENE GLYCOL  
METHYLPARABEN  
DIAZOLIDINYL UREA  
TROLAMINE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 55118-541-88 236 mL In 1 BOTTLE, PLASTIC None
2 55118-541-99 472 mL In 1 BOTTLE, PLASTIC None
3 55118-541-11 45 mL In 1 BOTTLE, PLASTIC None
4 55118-541-10 1000 mL In 1 BAG None
5 55118-541-12 1200 mL In 1 BAG None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333E 03/01/2023

Labeler - Kimberly-Clark Corporation (006072136)
Revised: 03/2013Kimberly-Clark Corporation