KAY MCD- chloroxylenol solution

Kay McD by

Drug Labeling and Warnings

Kay McD by is a Otc medication manufactured, distributed, or labeled by Kay Chemical Company. 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 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

INGREDIENTS AND APPEARANCE

KAY MCD 
chloroxylenol solution

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

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

Inactive Ingredients
Ingredient Name	Strength
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)
COCO GLUCOSIDE (UNII: ICS790225B)
GLYCERYL OLEATE (UNII: 4PC054V79P)
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)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63146-102-01	3800 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/13/2005

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	10/13/2005

Labeler - Kay Chemical Company (003237021)