Active ingredient

Chloroxylenol 0.5%

Purpose

Antiseptic handwash

Uses

For handwashing to decrease bacteria on the skin
recommended for repeated use.

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

for additional information, see Safety Data Sheet (SDS)
for emergency medical information in USA and Canada, call 1 800 328 0026. If located outside the United States and Canada, call collect 1 651 222 5352 (number is in the US)

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? call 1 866 781 8787

Principal display panel and representative label

NDC 47593-501-41 ECOLAB

Medi-Stat

Antimicrobial Hand Soap

Healthcare Personnel Handwash

Active Ingredient: Chloroxylenol 0.5%

6000077

Net Contents:

25 US fl oz (750 mL)

Ecolab · 1 Ecolab Place · St. Paul MN 55102 USA

Made in United States

www.ecolab.com · 755056/8501/0422

representative label

ECOLAB
chloroxylenol solution

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

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

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
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	10/06/2024
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	05/18/2023
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 Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	10/24/2012

Labeler - Ecolab Inc. (006154611)

Drug Facts