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

wash hands to remove soil
dispense palmful
spread to cover hands, rub in well
air dry, do not rinse or towel dry

Other information

for additional infomration see Safety Data Sheet (SDS)
EMERGENCY HEALTH INFORMATION: 1 877 231 2615. If located outside the United States and Canada, call collect 952 853 1713 (number is in the US).

Inactive ingredients water (aqua), potassium cocoate, hexylene glycol, sodium sulfate, tetrasodium edta, sodium lauryl sulfate, glycerin, sodium citrate, glyceryl oleate, fragrance, sodium glycolate, caprylyl/capryl glucoside, lauryl glucoside, magnesium nitrate, sodium hydroxide, methylchloroisothiazolinone, magnesium chloride, yellow 5, methylisothiazolinone, red 4

Questions? call 1-800-529-5458

Principal display panel and representative label

ECOLAB

NDC 63146-319-16

Foaming AB Hand Soap

Active Ingredient: Chloroxylenol 0.5%

1200 mL

(40.6 US FL OZ) 1112846

Kay Chemical Company · 8300 Capital Drive

Greensboro, NC 27409-9790 USA

Customer Service: (800) 529-5458

KUSA · 782978/8000/0224

representative label

ECOLAB FOAMING AB HS
chloroxylenol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:63146-319
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 (UNII: 0YPR65R21J)
EDETATE SODIUM (UNII: MP1J8420LU)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
GLYCERYL OLEATE (UNII: 4PC054V79P)
SODIUM GLYCOLATE (UNII: B75E535IMI)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
MAGNESIUM NITRATE (UNII: 77CBG3UN78)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
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:63146-319-16	1200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/19/2024

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	06/19/2024

Labeler - Kay Chemical Company (003237021)

Drug Facts