SCOTT ANTISEPTIC SKIN CLEANSER- chloroxylenol solution

Scott Antiseptic Skin Cleanser by

Drug Labeling and Warnings

Scott Antiseptic Skin Cleanser 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 1.25%

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 mediccal help or contact a Poison Control Center immediately.

Directions

Wet hands and apply a palmful. 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 Lauryl Sulfate, Acrylates/Steareth-20 Methacrylate Copolymer, Hexylene Glycol, Sodium C14-16 Olefin Sulfonate, Glycol Stearate, Fragrance, Sodium Hydroxide, 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 - 500 mL Carton

93036

Scott*
BRAND

Antiseptic Skin Cleanser

Chloroxylenol 1.25%

DIN: XXXXXXXX

500 mL (16.9 fl oz)

INGREDIENTS AND APPEARANCE

SCOTT ANTISEPTIC SKIN CLEANSER 
chloroxylenol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55118-245
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Chloroxylenol (UNII: 0F32U78V2Q) (Chloroxylenol - UNII:0F32U78V2Q)	Chloroxylenol	1.25 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Sodium Laureth-3 Sulfate (UNII: BPV390UAP0)
Hexylene Glycol (UNII: KEH0A3F75J)
Sodium C14-16 Olefin Sulfonate (UNII: O9W3D3YF5U)
Glycol Stearate (UNII: 0324G66D0E)
Sodium Hydroxide (UNII: 55X04QC32I)
Methylchloroisothiazolinone (UNII: DEL7T5QRPN)
Methylisothiazolinone (UNII: 229D0E1QFA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55118-245-05	500 mL in 1 BAG; Type 0: Not a Combination Product
2	NDC: 55118-245-08	800 mL in 1 BAG; 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)