SCOTT ANTISEPTIC FOAM SKIN CLEANSER- chloroxylenol solution

SCOTT Antiseptic Foam Skin Cleanser by

Drug Labeling and Warnings

SCOTT Antiseptic Foam Skin Cleanser by is a Otc medication manufactured, distributed, or labeled by Kimberly-Clark. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Chloroxylenol 1.75 %

Purpose

Antiseptic skin cleanser

Warnings

For external use only

Do not use if you are allergic to any of the ingredients

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

Stop use and ask a doctor if irritation develops

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

Directions

For occasional personal domestic use as needed. Supervise children when they use this product. Lather in hands with water for at least 30 seconds. Rinse well

Inactive ingredients

Water, Hexylene Glycol, Sodium Laureth Sulfate, Cocamidopropyl Betaine, Disodium EDTA, Sodium Hydroxide, Methylchloroisothiazolinone, Methylisothiazolinone

Questions?

Call 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 - 1.2 L Bottle Label

91595

Empty &
Discard Pump
PLASTIC
BOTTLE
how2recycle.info

DIN 02481286

For Personal / Domestic Use Only

Scott®
Brand

Antiseptic
Foam Skin Cleanser

Chloroxylenol Solution

SAME GREAT
FORMULATION.
Now Scott®
branded!

RINSE OFF

20-14-698-0-01

1.2 L (40.5 fl oz)

INGREDIENTS AND APPEARANCE

SCOTT ANTISEPTIC FOAM SKIN CLEANSER 
chloroxylenol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55118-900
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Chloroxylenol (UNII: 0F32U78V2Q) (Chloroxylenol - UNII:0F32U78V2Q)	Chloroxylenol	17.5 g  in 1 L

Inactive Ingredients
Ingredient Name	Strength
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
Water (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55118-900-63	6 in 1 CARTON	11/16/2018
1	NDC: 55118-900-10	1 L in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 55118-900-65	2 in 1 CARTON	11/16/2018
2	NDC: 55118-900-12	1.2 L in 1 BOTTLE; 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	11/16/2018

Labeler - Kimberly-Clark (830997032)