FOAMING AB HANDSOAP

Manufacturer: Ecolab Inc.
Effective date: 2025-12-30
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 01:29:41

Label at a glance#

ProductFOAMING AB HANDSOAP

Active ingredientCHLOROXYLENOL

Label structure9 sections

Indications and uses

For handwashing to decrease bacteria on the skin

Dosage and administration

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

Contacts and useful links#

PhoneLabel contact1 877 231 2615

PhoneLabel contact952 853 1713

PhoneLabel contact1-800-529-5458

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Chloroxylenol 0.5%

Purpose

OTC - PURPOSE SECTION

Antiseptic handwash

Uses

INDICATIONS & USAGE SECTION

For handwashing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

In eyes

When using this product

OTC - WHEN USING SECTION

If in eyes, rinse promptly and thoroughly with water
Discontinue use if irritation and redness develop

Stop use and ask a doctor if

OTC - ASK DOCTOR SECTION

skin irritation or redness occurs for more than 72 hours

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

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

Other information

REFERENCES SECTION

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 INGREDIENT SECTION

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

OTC - QUESTIONS SECTION

Questions? call 1-800-529-5458

Principal display panel and representative label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ECOLAB

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

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
436367	chloroxylenol 0.5 % Medicated Liquid Soap	PSN	1
436367	chloroxylenol 5 MG/ML Medicated Liquid Soap	SCD	1
436367	chloroxylenol 0.5 % Medicated Liquid Soap	SY	1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
362d7abb-94e6-4c60-9a58-266894157713	Product name	1	20231023
6bd95106-a412-1dad-b9cc-4cb74bfb27ce	Product name	2	20230315
7cda52fc-125f-421c-8fea-bc1974370c49	Product name	2	20180703
d5e51f11-ad28-caa4-4b49-4143974782ad	Product name	1	20150831
290f523a-f9db-9774-b5a9-e1f908ac1782	Product name	1	20150828
c6b65c52-69c7-df49-550a-a50c137f6218	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
47593-691-70	FOAMING AB HANDSOAP	1200 mL in 1 BOTTLE, PLASTIC	LIQUID	1200		1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 21 matching rows.

FOAMING AB HANDSOAP
Chloroxylenol
WATER
POTASSIUM COCOATE
HEXYLENE GLYCOL
SODIUM SULFATE
EDETATE SODIUM
SODIUM LAURYL SULFATE
GLYCERIN
SODIUM CITRATE
GLYCERYL OLEATE
SODIUM GLYCOLATE
DECYL GLUCOSIDE
LAURYL GLUCOSIDE
MAGNESIUM NITRATE
SODIUM HYDROXIDE
METHYLCHLOROISOTHIAZOLINONE
MAGNESIUM CHLORIDE
FD&C YELLOW NO. 5
METHYLISOTHIAZOLINONE
FD&C RED NO. 4

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
47593-691	47593-691-70

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
CHLOROXYLENOL	0F32U78V2Q	ACTIB
WATER	059QF0KO0R	IACT
POTASSIUM COCOATE	F8U72V8ZXP	IACT
HEXYLENE GLYCOL	KEH0A3F75J	IACT
SODIUM SULFATE	0YPR65R21J	IACT
EDETATE SODIUM	MP1J8420LU	IACT
SODIUM LAURYL SULFATE	368GB5141J	IACT
GLYCERIN	PDC6A3C0OX	IACT
SODIUM CITRATE	1Q73Q2JULR	IACT
GLYCERYL OLEATE	4PC054V79P	IACT
SODIUM GLYCOLATE	B75E535IMI	IACT
DECYL GLUCOSIDE	Z17H97EA6Y	IACT
LAURYL GLUCOSIDE	76LN7P7UCU	IACT
MAGNESIUM NITRATE	77CBG3UN78	IACT
SODIUM HYDROXIDE	55X04QC32I	IACT
METHYLCHLOROISOTHIAZOLINONE	DEL7T5QRPN	IACT
MAGNESIUM CHLORIDE	02F3473H9O	IACT
FD&C YELLOW NO. 5	I753WB2F1M	IACT
METHYLISOTHIAZOLINONE	229D0E1QFA	IACT
FD&C RED NO. 4	X3W0AM1JLX	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
d651eb4b-3618-4671-9922-5bfed4e1c9e6			f7da7470-3fbe-4869-8333-16d2091de53f	2025-12-30	Warnings	Exact identifier spl id: d651eb4b-3618-4671-9922-5bfed4e1c9e6 spl set id: f7da7470-3fbe-4869-8333-16d2091de53f

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.