KLEENEX HAND SANITIZER- alcohol 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® Hand Sanitizer Gel

Drug Facts

Active Ingredient

Ethyl Alcohol, 70%

Purpose

Antiseptic

Use

Hand sanitizer to decrease bacteria on the skin.

Warnings

Flammable - Keep product away from fire or flame. For external use only.

When using this product avoid contact with eyes. In case of contact, flush eyes with water.

Stop use & consult a health care practitioner if irritation or redness develops or persists.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

Wet hands thoroughly with product. Rub hands together briskly until dry.

Other Information

Report serious side effects from this product to 1-877-561-6587 Do not store above 37.8 C / 100 F

Inactive Ingredients

Carbopol 1342, Glycerol, Orange Flower Oil, Propylene Glycol, Triethanolamine, Water

Questions?

1-888-346-4652

PRINCIPAL DISPLAY PANEL - 50 mL Bottle Label

Kleenex ® BRAND

Hand Sanitizer Gel

Kills 99.9% of germs

1.7 fl oz / 50 mL

Principal Display Panel - 50 mL Bottle Label
KLEENEX HAND SANITIZER 
alcohol solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55118-610
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M) Alcohol70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
Carbomer Copolymer Type B (Allyl Pentaerythritol Crosslinked) (UNII: 809Y72KV36)  
Glycerin (UNII: PDC6A3C0OX)  
Citrus Sinensis Flower Oil (UNII: AJ56JP5TFP)  
Propylene Glycol (UNII: 6DC9Q167V3)  
Trolamine (UNII: 9O3K93S3TK)  
Water (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55118-610-5050 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart333E09/01/2013
Labeler - Kimberly-Clark Corporation (006072136)

Revised: 11/2014
Document Id: 05132d26-2d7a-4c1a-8f85-b500a1b63fde
Set id: 794c8f1f-bb5a-43b9-92c3-5f98b7f370ef
Version: 2
Effective Time: 20141103
 
Kimberly-Clark Corporation