SCOTT MOISTURIZING INSTANT HAND SANITIZER- alcohol solution

Scott by

Drug Labeling and Warnings

Scott by is a Otc medication manufactured, distributed, or labeled by Kimberly-Clark Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

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

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

Questions?

1-888-346-4652

SPL UNCLASSIFIED SECTION

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

PRINCIPAL DISPLAY PANEL - 500 mL Bottle Label

93044

Scott*
BRAND

Moisturizing Instant
Hand Sanitizer

Ethyl Alcohol 62%

NPN: XXXXXXX

500 mL (16.9 fl oz)

INGREDIENTS AND APPEARANCE

SCOTT   MOISTURIZING INSTANT HAND SANITIZER
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55118-325
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)
.ALPHA.-Tocopherol Acetate (UNII: 9E8X80D2L0)
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: 55118-325-05	500 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	03/01/2012

Labeler - Kimberly-Clark Corporation (006072136)