SCOTT CLEAR ANTIBACTERIAL SKIN CLEANSER- triclosan solution

Scott Clear Antibacterial Skin Cleanser by

Drug Labeling and Warnings

Scott Clear Antibacterial 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

Triclosan 0.25%

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 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 Beteine, Glycerin, Propylene Glycol, Frangrance, DL-Panthenol, Aloe Barbadensis Leaf Juice, Citric Acid, Methylchloroisothiazolinone, Methylisothiazolinone, Cocamide DEA.

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 - 500 mL Carton

92517

Scott*
BRAND

Clear Antibacterial Skin Cleanser

Triclosan 0.25%

DIN: 02369818

500 mL (16.9 fl oz)

INGREDIENTS AND APPEARANCE

SCOTT CLEAR ANTIBACTERIAL SKIN CLEANSER 
triclosan solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55118-205
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Triclosan (UNII: 4NM5039Y5X) (Triclosan - UNII:4NM5039Y5X)	Triclosan	0.25 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Sodium Laureth-3 Sulfate (UNII: BPV390UAP0)
Sodium Chloride (UNII: 451W47IQ8X)
Cocamidopropyl Betaine (UNII: 5OCF3O11KX)
Coco Diethanolamide (UNII: 92005F972D)
Glycerin (UNII: PDC6A3C0OX)
Propylene Glycol (UNII: 6DC9Q167V3)
Panthenol (UNII: WV9CM0O67Z)
Aloe Vera Leaf (UNII: ZY81Z83H0X)
Citric Acid Monohydrate (UNII: 2968PHW8QP)
Methylchloroisothiazolinone (UNII: DEL7T5QRPN)
Methylisothiazolinone (UNII: 229D0E1QFA)
Water (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55118-205-05	500 mL in 1 BAG; Type 0: Not a Combination Product
2	NDC: 55118-205-08	800 mL in 1 BAG; Type 0: Not a Combination Product
3	NDC: 55118-205-10	1000 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)