Active ingredient

Chloroxylenol 0.5%

Purpose

Antiseptic handwash

Uses

For handwashing to decrease bacteria on the skin

Warnings

For external use only.

Do not use

In eyes

When using this product

If in eyes, rinse promptly and thoroughly with water
Discontinue use if irritation and redness develop

Stop use and ask a physician if

Skin irritation or redness occurs for more than 72 hours

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Wet hands and forearms • Apply 5 ml (teaspoonful) or palmful to hands and forearms • Rub vigorously for 20 seconds • Wash between fingers, around fingernails and backs of hands • Rinse thoroughly with warm water Dry with paper towels or air-dry

Other Information

For additional information, see Safety Data Sheet (SDS)
For emergency medical information, call 866.897.8061

Inactive Ingredients Water (Aqua), Potassium Cocoate, Hexylene Glycol, Sodium Sulfate, Tetrasodium EDTA, Sodium lauryl sulfate, Hydroxyethylcellulose, Glycerin, Coco-glucoside, Glyceryl Oleate, fragrance, sodium glycolate, Sodium Hydroxide, Trisodium EDTA, Disodium EDTA, Sodium Citrate, Methylchloroisothiazolinone, Methylisothiazolinone, Red 40, Yellow 5, Red 33

Principal display panel and representative label

Member's Mark

COMMERCIAL

ANTIBACTERIAL

HAND SOAP

KILLS 99.9% OF GERMS*
FRESH, CLEAN FRAGRANCE
TRICLOSAN FREE

NET CONTENTS 1 GALLON (3.78 L)

Ecolab 4050 Corporate Drive, Ste. 100

Grapevine, Texas 76051 USA - 866.999.7484

DISTRIBUTED BY SAM'S WEST, INC.

BENTONVILLE, AR 72716

representative label

MEMBERS MARK
chloroxylenol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47593-573
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	5 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
POTASSIUM COCOATE (UNII: F8U72V8ZXP)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
SODIUM SULFATE (UNII: 0YPR65R21J)
EDETATE SODIUM (UNII: MP1J8420LU)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
HYDROXYETHYL CELLULOSE (2000 CPS AT 1%) (UNII: S38J6RZN16)
GLYCERIN (UNII: PDC6A3C0OX)
COCO GLUCOSIDE (UNII: ICS790225B)
GLYCERYL OLEATE (UNII: 4PC054V79P)
SODIUM GLYCOLATE (UNII: B75E535IMI)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
EDETATE TRISODIUM (UNII: 420IP921MB)
EDETATE DISODIUM (UNII: 7FLD91C86K)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
FD&C RED NO. 40 (UNII: WZB9127XOA)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:47593-573-11	3780 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/28/2016

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	07/28/2016

Labeler - Ecolab Inc. (006154611)

Drug Facts