ECOLAB- chloroxylenol solution

Ecolab by

Drug Labeling and Warnings

Ecolab by is a Otc medication manufactured, distributed, or labeled by Ecolab Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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 doctor 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 skin and spread a small amount on hands and forearms
• Scrub well, rinse thoroughly and dry

Other information

• Read Material Safety Data Sheet (MSDS) before using this product
• Emergency Healthcare Information:  1 800 328 0026.  If located outside the United States and Canada, call collect 1 651 222 5352 (number is in the US)

INACTIVE INGREDIENT

Inactive ingredients  water (aqua), potassium cocoate, hexylene glycol, sodium sulfate, tetrasodium EDTA, sodium lauryl sulfate, hydroxyethylcellulose, glycerin, cocoglucoside, glyceryl oleate, citric acid, frangrance, methylchloroisothiazolinone, methylisothiazolinone, FD&C red #40, FD&C yellow #5, D&C red #33

QUESTIONS

Questions? call 1 800 781 8787

Principal Display Panel and Representative Label

ECOLAB

NDC: 47593-501-31

MEDI-STAT™

Anitmicrobial Hand Soap

Active Ingredient: 0.5% Chloroxylenol

6000033

Net Contents:  540 mL (18 fl oz)

Ecolab · 370 Wabasha Street N ·

St Paul MN 55102-1390 USA

© 2012 Ecolab USA Inc · All rights reserved

Made in United States

www.ecolab.com · 753737/8500/1012

INGREDIENTS AND APPEARANCE

ECOLAB 
chloroxylenol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47593-501
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	5.20 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
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 (3000 CPS AT 1%) (UNII: 7Q6P4JN1QT)
GLYCERIN (UNII: PDC6A3C0OX)
COCO GLUCOSIDE (UNII: ICS790225B)
GLYCERYL OLEATE (UNII: 4PC054V79P)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
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)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 47593-501-31	540 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/24/2012
2	NDC: 47593-501-32	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/24/2012
3	NDC: 47593-501-26	1000 mL in 1 POUCH; Type 0: Not a Combination Product	10/25/2012
4	NDC: 47593-501-11	3780 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/26/2012
5	NDC: 47593-501-56	1200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/26/2012
6	NDC: 47593-501-41	750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/22/2013
7	NDC: 47593-501-59	1250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/23/2013

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	10/24/2012

Labeler - Ecolab Inc. (006154611)