KLEENEX MOISTURIZING HAND SANITIZER, HYDRATES SKIN- alcohol solution

Kleenex Moisturizing Hand Sanitizer, Hydrates Skin by

Drug Labeling and Warnings

Kleenex Moisturizing Hand Sanitizer, Hydrates Skin by is a Otc medication manufactured, distributed, or labeled by Kimberly-Clark Corporation, Marietta Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Medicinal Ingredient

Ethyl Alcohol, 62% v/v

Purpose

Antiseptic

Use

Antiseptic cleanser. Kills harmful bacteria or germs.

Warnings

FLAMMABLE. Keep away from open flame and sources of heat.

For External Use Only.

WHEN USING

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

STOP USE

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

KEEP OUT OF REACH OF CHILDREN

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. Use as part of your daily cleansing routine.

Other Information

Report serious side effects from this product to 1-877-561-6587. Do not store above 110°F (40°C).

Non-Medicinal Ingredients

Water/Eau, Betaine, Fragrance/Parfum, Meadowfoamamidopropyl Betaine, PEG-7 Glyceryl Cocoate, PEG-10 Dimethicone.

Questions?

1-888-346-4652

SPL UNCLASSIFIED SECTION

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

MARQUE
Kleenex®
BRAND

Moisturizing Foam
Hand Sanitizer

hydrates
skin

NPN: 80015523

For Personal / Domestic Use Only

1 Liter (33.8 fl oz)

20-14-708-0-00

INGREDIENTS AND APPEARANCE

KLEENEX MOISTURIZING HAND SANITIZER, HYDRATES SKIN 
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55118-545
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M)	Alcohol	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Betaine (UNII: 3SCV180C9W)
Peg-7 Glyceryl Cocoate (UNII: VNX7251543)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55118-545-88	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
2	NDC: 55118-545-99	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
3	NDC: 55118-545-11	45 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
4	NDC: 55118-545-10	1000 mL in 1 BAG; Type 0: Not a Combination Product
5	NDC: 55118-545-12	1200 mL in 1 BAG; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part333E	03/01/2012

Labeler - Kimberly-Clark Corporation (006072136)

Establishment
Name	Address	ID/FEI	Business Operations
Marietta Corporation		010765394	MANUFACTURE(55118-545) , ANALYSIS(55118-545) , RELABEL(55118-545)