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 infomration 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, glycerin, sodium citrate, glyceryl oleate, fragrance, sodium glycolate, caprylyl/capryl glucoside, lauryl glucoside, magnesium nitrate, sodium hydroxide, methylchloroisothiazolinone, magnesium chloride, yellow 5, methylisothiazolinone, red 4

Questions? call 1 866 781 8787

Principal display panel and representative label

NDC 47593-503-59

ECOLAB

MEDI-STAT® Foam

Antimicrobial Hand Soap

Active Ingredient: Chloroxylenol 0.5%

Net Contents: 1250 mL (42.3 fl oz)

6000107

Ecolab · 1 Ecolab Place · St Paul MN 55102 USA

Made in United States

755670/8502/0422

representative label

ECOLAB INC.
chloroxylenol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47593-503
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)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
GLYCERYL OLEATE (UNII: 4PC054V79P)
SODIUM GLYCOLATE (UNII: B75E535IMI)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
MAGNESIUM NITRATE (UNII: 77CBG3UN78)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:47593-503-41	750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/27/2013
2	NDC:47593-503-59	1250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/27/2013

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	10/27/2013

Labeler - Ecolab Inc. (006154611)

Drug Facts