KLEENEX REVEAL MOISTURIZING FOAM HAND SANITIZER- alcohol solution

Kleenex Reveal Moisturizing Foam Hand Sanitizer by

Drug Labeling and Warnings

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

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

Ethyl Alcohol 70%

Purpose

Antimicrobial

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 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
• Do not store above 110° F (40° C).

inactive Ingredients

Aloe Barbadensis Leaf Extract, Betaine, Camellis Sinensis Leaf Extract, Citric Acid, Cucumis Sativus (Cucumber) Fruit Extract, Isooropanol, Glycerin, Meadowfoamamidopropyl Betaine, Panthenol, PEG-10 Dimethicone, Water

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 - 45 mL Bottle Label

Kleenex® BRAND

REVEAL™
MOISTURIZING FOAM
HAND SANITIZER

ULTRA

NPN: 80030706

For Personal / Domestic Use Only

1.5 fl oz (45 mL)

INGREDIENTS AND APPEARANCE

KLEENEX REVEAL MOISTURIZING FOAM HAND SANITIZER 
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55118-531
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M)	Alcohol	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
Betaine (UNII: 3SCV180C9W)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
CUCUMBER (UNII: YY7C30VXJT)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
Glycerin (UNII: PDC6A3C0OX)
Meadowfoamamidopropyl Betaine (UNII: HNV0L650LG)
Panthenol (UNII: WV9CM0O67Z)
PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
Water (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55118-531-64	24 in 1 CARTON	05/15/2018
1	NDC: 55118-531-11	45 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 55118-531-67	4 in 1 CARTON	05/15/2018
2	NDC: 55118-531-18	532 mL in 1 BOTTLE; 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	05/15/2018

Labeler - Kimberly-Clark (830997032)