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 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 (FD&C Yellow No. 5), methylisothiazolinone, CI 14700 (FD&C Red. No. 4)

Questions? Call 1-800-529-5458

Representative Label and Principal Display Panel

ECOLAB®

Peel Here For Drug Facts

NDC 63146-124-10

Foaming Antibacterial
Hand Soap
Jabón de manos
antibacterial en espuma

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.
Para obtener las instrucciones en español, véase la caja exterior.

Net contents: 42 US fl oz (1250 ml)

representative label

ECOLAB
chloroxylenol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:63146-124
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 ANHYDROUS (UNII: 36KCS0R750)
EDETATE SODIUM (UNII: MP1J8420LU)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
GLYCERIN (UNII: PDC6A3C0OX)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
COCO-GLUCOSIDE (UNII: ICS790225B)
GLYCERYL OLEATE (UNII: 4PC054V79P)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:63146-124-10	1250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/30/2015

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	12/30/2015

Labeler - Kay Chemical Company (003237021)