KLEENEX MOISTURIZING INSTANT HAND SANITIZER- alcohol solution

Kleenex Moisturizing Instant Hand Sanitizer by

Drug Labeling and Warnings

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

Drug Details [pdf]

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Drug Facts

Active Ingredient

Ethyl Alcohol 62%

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 & 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 right away.

Directions

Wet hands thoroughly with product and allow to dry.

Other Information

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

Inactive Ingredients

Water, Glycerin, Dimethicone, Carbomer, Petrolatum, Aminomethyl Propanol, Fragrance, Tocopheryl Acetate, Panthenol, Hydroxypropylcellulose, Ceteth-10, Steareth-21, Poloxamer 335, Aloe Barbadensis Leaf

Questions?

1-888-346-4652

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

www.kcprofessional.com

PRINCIPAL DISPLAY PANEL - 1.5 mL Pouch Label

MARQUE
Kleenex*
BRAND

Moisturizing Instant
Hand Sanitizer

Contains Aloe & Vitamin E

Single Use

.05
Fl Oz
(1.5 mL)

INGREDIENTS AND APPEARANCE

KLEENEX MOISTURIZING INSTANT HAND SANITIZER 
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55118-480
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)
Glycerin (UNII: PDC6A3C0OX)
Dimethicone (UNII: 92RU3N3Y1O)
Petrolatum (UNII: 4T6H12BN9U)
Aminomethylpropanol (UNII: LU49E6626Q)
Panthenol (UNII: WV9CM0O67Z)
Hydroxypropyl Cellulose (Type H) (UNII: RFW2ET671P)
Ceteth-10 (UNII: LF9X1PN3XJ)
Steareth-21 (UNII: 53J3F32P58)
Poloxamer 335 (UNII: G6DQL26D50)
Aloe Vera Leaf (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55118-480-10	1000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product
2	NDC: 55118-480-88	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
3	NDC: 55118-480-22	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
4	NDC: 55118-480-12	1200 mL in 1 CARTRIDGE; Type 0: Not a Combination Product
5	NDC: 55118-480-55	15 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
6	NDC: 55118-480-11	30 mL in 1 BOTTLE, PLASTIC; 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	03/01/2011

Labeler - Kimberly-Clark Corporation (006072136)

Establishment
Name	Address	ID/FEI	Business Operations
Marietta Corporation		010765394	MANUFACTURE(55118-480) , ANALYSIS(55118-480) , RELABEL(55118-480)