KLEENEX ALCOHOL FREE FOAM HAND SANITIZER- 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® 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 TypeHUMAN OTC DRUG LABELItem Code (Source)NDC:55118-541
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Benzalkonium Chloride (Benzalkonium) Benzalkonium Chloride1.3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
ALLANTOIN 
CETRIMONIUM CHLORIDE 
COCAMIDOPROPYL BETAINE 
COCAMIDOPROPYLAMINE OXIDE 
DIDECYLDIMETHYLAMMONIUM CHLORIDE 
PROPYLPARABEN 
PROPYLENE GLYCOL 
METHYLPARABEN 
DIAZOLIDINYL UREA 
TROLAMINE 
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55118-541-88236 mL in 1 BOTTLE, PLASTIC
2NDC:55118-541-99472 mL in 1 BOTTLE, PLASTIC
3NDC:55118-541-1145 mL in 1 BOTTLE, PLASTIC
4NDC:55118-541-101000 mL in 1 BAG
5NDC:55118-541-121200 mL in 1 BAG
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E03/01/2013
Labeler - Kimberly-Clark Corporation (006072136)

Revised: 3/2013
Document Id: d876c7ec-b2d6-4769-9748-9315b32a6a91
Set id: 4334dcfc-50f0-49a9-a40f-6d94f6fef2ed
Version: 1
Effective Time: 20130306
 
Kimberly-Clark Corporation