SCOTT ANTIBACTERIAL SKIN CLEANSER- chloroxylenol 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

Chloroxylenol 0.5%

Purpose

Antiseptic

Use

For handwashing to decrease bacteria on the skin.

Warnings

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

Wet hands and apply a palmful to hands. Scrub thoroughly for 15-20 seconds.

Rinse and dry thoroughly.

Other Information

• Report serious side effects from this product to 1-877-561-6587

Inactive Ingredients

Water, Sodium Laureth Sulfate, Sodium Chloride, Cocamidopropyl Betaine, Propylene Glycol, Fragrance, Ethanolamine, Citric Acid, Methylchloroisothiazolinone, Methylisothiazolinone

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 - 800 mL Container Label

91298

Scott*
BRAND

Antibacterial Skin Cleanser

Chloroxylenol 0.5%

DIN: XXXXXXXX

800 mL (27 fl oz)

INGREDIENTS AND APPEARANCE

SCOTT   ANTIBACTERIAL SKIN CLEANSER
chloroxylenol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55118-225
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Chloroxylenol (UNII: 0F32U78V2Q) (Chloroxylenol - UNII:0F32U78V2Q)	Chloroxylenol	0.5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Sodium Laureth-3 Sulfate (UNII: BPV390UAP0)
Sodium Chloride (UNII: 451W47IQ8X)
Cocamidopropyl Betaine (UNII: 5OCF3O11KX)
Coco Diethanolamide (UNII: 92005F972D)
Propylene Glycol (UNII: 6DC9Q167V3)
Monoethanolamine (UNII: 5KV86114PT)
Citric Acid Monohydrate (UNII: 2968PHW8QP)
Methylchloroisothiazolinone (UNII: DEL7T5QRPN)
Methylisothiazolinone (UNII: 229D0E1QFA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55118-225-08	800 mL in 1 BAG; Type 0: Not a Combination Product
2	NDC: 55118-225-01	3785 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)