SCOTT MOISTURIZING FOAM HAND SANITIZER- alcohol solution

Scott Moisturizing Foam Hand Sanitizer by

Drug Labeling and Warnings

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

Stop use & ask 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

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).

Inactive 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 - 33.8 fl oz Bottle Label

91560

SAME GREAT
FORMULATION.
Now Scott®
branded!

Scott®
Brand

Moisturizing Foam
Hand Sanitizer

Hydrates skin

LEAVE ON

20-14-708-0-01

Empty &
Discard Pump

PLASTIC
BOTTLE

how2recycle.info

NPN: 80015523

For Personal / Domestic Use Only

1 Liter (33.8 fl oz)

INGREDIENTS AND APPEARANCE

SCOTT MOISTURIZING FOAM HAND SANITIZER 
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55118-546
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)
Meadowfoamamidopropyl Betaine (UNII: HNV0L650LG)
PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)
PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55118-546-63	6 in 1 CARTON	04/16/2018
1	NDC: 55118-546-10	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 55118-546-65	2 in 1 CARTON	04/16/2018
2	NDC: 55118-546-12	1200 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	04/16/2018

Labeler - Kimberly-Clark (830997032)