AFCO 5508 Sanifect Foam-E II

Manufacturer: Zep Inc.
Effective date: 2025-12-26
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 01:28:50

Label at a glance#

ProductAFCO 5508 Sanifect Foam-E II

Active ingredientCHLOROXYLENOL

Label structure12 sections

Indications and uses

For handwashing to decrease bacteria on the skin. Recommended for repeated use.

Dosage and administration

Wet hands with water, apply enough product to cover all hand surfaces, rub hands together for at least 30 seconds to work into lather. Rinse thoroughly and dry hands completely.

Contacts and useful links#

PhoneLabel contact1-877-428-9937

Websitewww.zep.com

www.zep.com

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Chloroxylenol 1.0% w/w

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

For handwashing to decrease bacteria on the skin.
Recommended for repeated use.

Warnings

WARNINGS SECTION

FOR EXTERNAL USE ONLY

When using this product

OTC - WHEN USING SECTION

When using this product avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

Stop use and ask a doctor if if irritation or redness develops and persists.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact poison control center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands with water, apply enough product to cover all hand surfaces, rub hands together for at least 30 seconds to work into lather.
Rinse thoroughly and dry hands completely.

Other information

OTHER SAFETY INFORMATION

For Food Processing, Food Service and Professional Use Only.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Ammonium Lauryl Sulfate, Ethanol, Sodium Lauroyl Sarcosinate, Triethylene Glycol, Propylene Glycol, Glycerin, Disodium EDTA, Cocomidopropyl Hydroxysultaine, Citric Acid, Cocamide MIPA.

Questions or comments?

OTC - QUESTIONS SECTION

For product or technical information, contact ZEP, INC. Monday to Friday 8 AM to 4 PM EST at 1-877-428-9937 or visit our website at www.zep.com.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

139 AF5508

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
413257	chloroxylenol 1 % Medicated Liquid Soap	PSN	1
413257	chloroxylenol 10 MG/ML Medicated Liquid Soap	SCD	1
413257	chloroxylenol 1 % Medicated Liquid Soap	SY	1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
66949-141-01	AFCO 5508 Sanifect Foam-E II	208198 mL in 1 DRUM	LIQUID	208198	1
66949-141-02	AFCO 5508 Sanifect Foam-E II	6000 mL in 1 CASE	LIQUID	6000	1
66949-141-03	AFCO 5508 Sanifect Foam-E II	3785 mL in 1 CASE	LIQUID	3785	1

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

AFCO 5508 Sanifect Foam-E II
Chloroxylenol
SODIUM LAUROYL SARCOSINATE
COCAMIDOPROPYL HYDROXYSULTAINE
GLYCERIN
WATER
AMMONIUM LAURYL SULFATE
PROPYLENE GLYCOL
EDETATE DISODIUM
ALCOHOL
COCAMIDE MEA
TRIETHYLENE GLYCOL
CITRIC ACID

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
66949-141	66949-141-01, 66949-141-02, 66949-141-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
SODIUM LAUROYL SARCOSINATE	632GS99618	IACT
COCAMIDOPROPYL HYDROXYSULTAINE	62V75NI93W	IACT
GLYCERIN	PDC6A3C0OX	IACT
WATER	059QF0KO0R	IACT
AMMONIUM LAURYL SULFATE	Q7AO2R1M0B	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
EDETATE DISODIUM	7FLD91C86K	IACT
ALCOHOL	3K9958V90M	IACT
COCAMIDE MEA	C80684146D	IACT
CHLOROXYLENOL	0F32U78V2Q	ACTIB
TRIETHYLENE GLYCOL	3P5SU53360	IACT
CITRIC ACID	2968PHW8QP	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
AFCO 5508 Sanifect Foam-E II	CHLOROXYLENOL	Zep Inc.	46deac5c-97e8-8924-e063-6294a90a5dbc	2025-12-26	Warnings	Exact identifier ndc (package): 66949-141-03 ndc (package): 66949-141-01 ndc (package): 66949-141-02 ndc (product): 66949-141 ndc11 (package): 66949014101 ndc11 (package): 66949014102 ndc11 (package): 66949014103 spl id: 46deac6a-c618-0da2-e063-6394a90a02c2 spl set id: 46deac5c-97e8-8924-e063-6294a90a5dbc

Reported adverse events (FAERS/openFDA)#

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