KAY MCD- chloroxylenol solution 
Kay Chemical Company

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active ingredient

Chloroxylenol 0.5%

Purpose

Antiseptic handwash

Uses

Warnings

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

Other information

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 TypeHUMAN OTC DRUGItem Code (Source)NDC:63146-102
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL0.5 mg  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63146-102-013800 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/13/2005
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E10/13/2005
Labeler - Kay Chemical Company (003237021)

Revised: 7/2022
Document Id: c363ff99-ff66-4e36-a454-fc9db7c71802
Set id: 10c061e8-ff72-4de8-897d-745199b8263a
Version: 5
Effective Time: 20220726
 
Kay Chemical Company