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KLEENEX Foam Hand Sanitizer, Alcohol Free

Dosage form: solution
Ingredients: Benzalkonium Chloride 0.001g in 1mL
Labeler: Kimberly-Clark Corporation
NDC Code: 55118-540

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 FOAM HAND SANITIZER, ALCOHOL FREE

Drug Facts

Active Ingredient

Benzalkonium Chloride 0.1%

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

Inactive Ingredients

Behentrimonium chloride, Dihydroxyethyl cocamine oxide, Dihydroproyl PEG-5 linoleammonium chloride, Glycereth -2 cocoate, Water

Questions?

1-888-346-4652

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

PRINCIPAL DISPLAY PANEL - 236 mL Bottle Label

Kleenex®
BRAND

Foam
Hand Sanitizer

alcohol
free

8 fl oz (236 mL)

20-14-633-0-00

KLEENEX FOAM HAND SANITIZER, ALCOHOL FREE 
benzalkonium chloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55118-540
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:55118-540-88236 mL in 1 BOTTLE, PLASTIC
2NDC:55118-540-99473 mL in 1 BOTTLE, PLASTIC
3NDC:55118-540-1145 mL in 1 BOTTLE, PLASTIC
4NDC:55118-540-101000 mL in 1 BAG
5NDC:55118-540-121200 mL in 1 BAG
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart333E03/01/2012
Labeler - Kimberly-Clark Corporation (006072136)

Revised: 02/2012
Document Id: 397214ce-e77f-4122-aa58-25936c0c8979
Set id: 27733190-4038-4dc2-b89f-5f4bfdf7fe4c
Version: 2
Effective Time: 20120215
 
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 drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.

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