Drug Facts

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 and 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.
Scrub thoroughly for 20 seconds.
Rinse and repeat.

Other information

For additional information, see Material Safety Data Sheet (MSDS)
For emergency medical information in USA call (877) 231-2615 or call collect 0 (952)853-1713.

Inactive ingredients

water (aqua), potassium cocoate, hexylene glycol, sodium sulfate, tetrasodium EDTA, sodium lauryl sulfate, hydroxyethylcellulose, glycerine, coco glucoside, glyceryl oleate, citric acid, fragrance, methylchloroisothiazolinone, methylisothiazolinone, FD&C Red 40, FD&C Yellow 5, D&C Red 33.

Questions?

Call 1-800-529-5458

Principal Display Panel - Representative Label

NDC No.: 63146-102-01

McD

Anti-Microbial

Handwash (AMH)

FOR INSTITUTIONAL USE ONLY

(Chloroxylenol 0.5%)

1 US gal (3.8L)

ECOLAB

KAY CHEMICAL COMPANY - 8300 Capital Drive - Greensboro, NC 27409-9790 USA

Customer Service: (800) 529-5458

Made in USA

Representative label

KAY MCD
chloroxylenol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:63146-102
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	0.5 mg in 100 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
POTASSIUM COCOATE (UNII: F8U72V8ZXP)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
SODIUM SULFATE ANHYDROUS (UNII: 36KCS0R750)
EDETATE SODIUM (UNII: MP1J8420LU)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
HYDROXYETHYL CELLULOSE (3000 MPA.S AT 1%) (UNII: 7Q6P4JN1QT)
GLYCERIN (UNII: PDC6A3C0OX)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
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:63146-102-01	3800 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/13/2005	12/31/2025

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	10/13/2005	12/31/2025

Labeler - Kay Chemical Company (003237021)

Revised: 12/2025

Document Id: 64bff050-236b-42e1-925a-37880e97c9e2

Set id: 10c061e8-ff72-4de8-897d-745199b8263a

Version: 7

Effective Time: 20251231

Kay Chemical Company