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 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 hands and forearms • Apply palmful of to hands and forearms
Scrub thoroughly • Rinse and dry

Other Information

for additional information, see Safety Data Sheet (SDS)
Medical Emergency: (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, glycerin, citric acid, coco-glucoside, glyceryl oleate, fragrance, methylchloroisothiazolinone, CI 19140 (FDC Yellow No. 5), methylisothiazolinone, CI 14700 (FDC Red No. 4)

Questions? Call 1-800-529-5458

Principal display panel and representative label

NDC 63146-108-10

Kay®

Peel Here For Drug Facts

McD® Foaming

Antibacterial Hand Soap

Instant foam lathers fast •Mild, pH-balanced formula •Fresh, clean fragrance

McD® Foaming Antibacterial Hand Soap is a rich lather hand soap with a balanced blend of cleaning agents and skin protecting moisturizers.

KEEP OUT OF REACH OF CHILDREN • FOR INSTITUTIONAL USE ONLY

Chloroxylenol 0.5%

To obtain Spanish Instructions, see outer carton.

Net contents: 42 US fl oz (1250 mL)

Distributed by:

KAY CHEMICAL COMPANY•8300 Capital Drive

Greensboro, NC 27409-9790, USA

Customer Service: (800) 529-5458

®2015 Kay Chemical Company

763982-00•McDUSA 763982/8000/1115

representative label

MCD
chloroxylenol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:63146-108
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 (UNII: 0YPR65R21J)
EDETATE SODIUM (UNII: MP1J8420LU)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
GLYCERIN (UNII: PDC6A3C0OX)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
GLYCERYL MONOOLEATE (UNII: C4YAD5F5G6)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)
COCO GLUCOSIDE (UNII: ICS790225B)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:63146-108-03	750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/17/2007	09/18/2019
2	NDC:63146-108-10	1250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/17/2007

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	08/17/2007

Labeler - Kay Chemical Company (003237021)