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 Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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Product Facts

Medicinal ingredient

Ethyl Alcohol 62% v/v

Purpose

Antiseptic cleanser

Uses

For personal hand hygiene to help prevent the spread of bacteria. Kills harmful bacteria or germs.

Warnings

For external use only

Flammability warning

Keep away from open flame and sources of heat.

When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if irritation or redness develops or persists.

Keep out of reach of children. If swallowed, get medical help or contact a poison control centre right away.

Directions

Use enough foam to cover your hands. Supervise children when they use this product. For occasional and personal domestic use. Rub thoroughly into hands for at least 30 seconds. Allow to 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

Betaine, Fragrance/Parfum, Meadowfoam Amidopropyl Betaine, PEG-10 Dimethicone, PEG-7 Gylceryl Cocoate, Water/Eau/Aqua

Questions?

1-888-346-4652

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Imported and distributed in Canada by Kimberly-Clark Inc.,
Mississauga, Ontario L5B 3Y5.

PRINCIPAL DISPLAY PANEL - 1.2 Liter Bottle Label

Scott®
Brand

SAME GREAT
FORMULATION.
Now Scott®
branded!

Moisturizing Foam Hand Sanitizer

Hydrates skin

LEAVE ON

1.2 Liters (40.5 fl oz)

INGREDIENTS AND APPEARANCE

SCOTT MOISTURIZING FOAM HAND SANITIZER 
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55118-703
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)
PEG-10 Dimethicone (600 CST) (UNII: 8PR7V1SVM0)
Betaine (UNII: 3SCV180C9W)
PEG-7 Glyceryl Cocoate (UNII: VNX7251543)
Meadowfoamamidopropyl Betaine (UNII: HNV0L650LG)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55118-703-12	1200 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	09/01/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	09/01/2015

Labeler - Kimberly-Clark Corporation (830997032)