KLEENEX FOAM HAND SANITIZER- benzalkonium chloride solution 
Kimberly-Clark

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® 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 bacteria

Warnings

For external use only. Do not ingest. Use with caution in children.

Do not use if you are allergic to any ingredients.

When using this product, avoid contact with eyes.

If contact occurs, rinse with water.

Stop use and ask a doctor if irritation develops.

Keep out of reach of children. If swallowed, call a poison control centre or get medical help right away.

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 and personal domestic use. Supervise children when they use this product.

Other information

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

Inactive ingredients

Aloe Barbadensis Leaf Juice Powder, 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 - 532 mL Bottle Label

Kleenex®

Foam Hand Sanitizer

alcohol
free

DIN: 02443252

For Personal / Domestic Use Only

18 fl oz (532 mL)

PRINCIPAL DISPLAY PANEL - 532 mL Bottle Label
KLEENEX FOAM HAND SANITIZER 
benzalkonium chloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55118-701
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Benzalkonium Chloride (UNII: F5UM2KM3W7) (Benzalkonium - UNII:7N6JUD5X6Y) Benzalkonium Chloride1.3 mg  in 1000 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Methylpropanediol (UNII: N8F53B3R4R)  
Cocamidopropyl Propylene Glycol-Dimonium Chloride Phosphate (UNII: H2KVQ74JM4)  
Polyethylene Oxide 600000 (UNII: 2126FD486L)  
Citric Acid Monohydrate (UNII: 2968PHW8QP)  
Silicon Dioxide (UNII: ETJ7Z6XBU4)  
Aloe (UNII: V5VD430YW9)  
Panthenol (UNII: WV9CM0O67Z)  
Sodium Hydroxide (UNII: 55X04QC32I)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55118-701-6424 in 1 CARTON09/01/2015
1NDC:55118-701-1145 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
2NDC:55118-701-99473 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product09/01/2015
3NDC:55118-701-101000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product09/01/2015
4NDC:55118-701-121200 mL in 1 CARTRIDGE; Type 0: Not a Combination Product09/01/2015
5NDC:55118-701-674 in 1 CARTON09/01/2015
5NDC:55118-701-18532 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart333E09/01/2015
Labeler - Kimberly-Clark (830997032)
Establishment
NameAddressID/FEIBusiness Operations
Tri-Pac Inc.020844956MANUFACTURE(55118-701) , LABEL(55118-701) , PACK(55118-701)
Establishment
NameAddressID/FEIBusiness Operations
Cyan Labs812754130MANUFACTURE(55118-701) , LABEL(55118-701) , ANALYSIS(55118-701) , PACK(55118-701)

Revised: 7/2023
Document Id: 67829125-8817-4922-8af8-6fb912c11697
Set id: 1fa77ae2-b652-463d-8943-d338c591226e
Version: 5
Effective Time: 20230712
 
Kimberly-Clark