KLEENEX Luxury Foam Hand Sanitizer

Dosage form: solution
Ingredients: Benzalkonium Chloride 0.001g in 1mL
Labeler: Kimberly-Clark Corporation
NDC Code: 55118-521

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.

MARQUE
Kleenex®
BRAND
LUXURY FOAM HAND SANITIZER

Drug Facts

Active Ingredient

Benzalkonium Chloride 0.1%

Purpose

Antiseptic

Use

Hand sanitizer to decrease bacteria on the skin. Recommended for repeated use.

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.

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

Directions

Pump enough foam product into your palm to cover your hands. Rub hands together briskly until dry. No rinsing required. Use as part of a daily cleaning routine.

Inactive / Non-medicinal Ingredients

Water, dihydroxypropyl PEG-5, linoleammonium chloride, glycereth-2 cocoate, behentrimonium chloride, dihydroxyethyl cocamine oxide

Questions?

1-800-346-4652

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 - 1 Liter Container Label

Kimberly-Clark
PROFESSIONAL*

MARQUE
kleenex®
BRAND

LUXURY FOAM HAND SANITIZER

Benzalkonium Chloride Solution, House Std., 0.1%

For Personal/Domestic Use Only

Fragrance Free • Alcohol Free

1 Liter
(33.8 fl oz)

NSF®

Nonfood Compounds
Program Listed E3
143923

NDC: 055118-521-10
DIN: 02366045

20-14-559-0-01

KLEENEX LUXURY FOAM HAND SANITIZER 
benzalkonium chloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55118-521
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Benzalkonium Chloride (Benzalkonium) Benzalkonium Chloride0.001 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
water 
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE 
GLYCERETH-2 COCOATE 
BEHENTRIMONIUM CHLORIDE 
DIHYDROXYETHYL COCAMINE OXIDE 
Packaging
#Item CodePackage Description
1NDC:55118-521-101000 mL in 1 CONTAINER
2NDC:55118-521-121200 mL in 1 CONTAINER
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart333E08/15/2011
Labeler - Kimberly-Clark Corporation (006072136)

Revised: 07/2011
 
Kimberly-Clark Corporation

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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