FDA.reportPublic FDA data

Zep FS Antimicrobial Foaming Hand Cleaner

Manufacturer
Zep Inc.
Effective date
2020-11-18
Label type
HUMAN OTC DRUG LABEL
Version
11
Source
legacy-cache
Hydrated at
2026-08-01 23:06:34

Label at a glance#

ProductZep FS Antimicrobial Foaming Hand Cleaner
Active ingredientBENZALKONIUM CHLORIDE
Label structure13 sections

Indications and uses

Hand washing to decrease bacteria on the skin. For use in food processing facilities.

Dosage and administration

Wet hands with water. Place hands under dispenser and apply liquid soap. Massage soap into hands and writsts, emphasizing back of hands, knuckles and cuticles. Rise hands thoroughly and dry.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic Hand Wash

Uses

INDICATIONS & USAGE SECTION

  • Hand washing to decrease bacteria on the skin.
  • For use in food processing facilities.

Warnings

WARNINGS SECTION

For external use only.

OTC - DO NOT USE SECTION

Do not use in the eyes; if in eyes, rinse promptly and thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask doctor if skin irritation or redness persists for more than 72 hours.

OTC - WHEN USING SECTION

  • Do not swallow.
  • If swallowed, do not induce vomiting and if individual is conscious, give large quantities of water to drink and consult a physician immediately.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children and pets. Children must be supervised in use of this product.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands with water.
  • Place hands under dispenser and apply liquid soap.
  • Massage soap into hands and writsts, emphasizing back of hands, knuckles and cuticles.
  • Rise hands thoroughly and dry.

Other information

OTHER SAFETY INFORMATION

  • Store at 20 to 25°C (68 to 77°F).
  • Do not freeze.
  • Dispose in accordance with all applicable federal, state and local regulations.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Cocamidopropyl Hydroxysultaine, Lauramine Oxide, Didecyldimonium Chloride, PEG-6 Cocamide, Phenoxyethanol, Iodopropynyl Butylcarbamate, Methylisothiazolinone, Hexanediol

Questions or comments?

OTC - QUESTIONS SECTION

Call 1-800-I-BUY-ZEP (1-800-428-9937)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

0996.jpg0996.jpg

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
BENZALKONIUM CHLORIDEACTIVE INGREDIENTF5UM2KM3W75
BENZALKONIUMACTIVE MOIETY7N6JUD5X6Y5
COCAMIDOPROPYL BETAINEINACTIVE INGREDIENT5OCF3O11KX5
DMDM HYDANTOININACTIVE INGREDIENTBYR0546TOW5
IODOPROPYNYL BUTYLCARBAMATEINACTIVE INGREDIENT603P14DHEB5
LAURAMINE OXIDEINACTIVE INGREDIENT4F6FC4MI8W5
PEG-6 COCAMIDEINACTIVE INGREDIENTYZ6NLA4O1E5
WATERINACTIVE INGREDIENT059QF0KO0R5

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
66949-99666949-996-11, 66949-996-16, 66949-996-85, 66949-996-17

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
HEXANEDIOLZIA319275IIACT
WATER059QF0KO0RIACT
COCAMIDOPROPYL HYDROXYSULTAINE62V75NI93WIACT
LAURAMINE OXIDE4F6FC4MI8WIACT
PEG-6 COCAMIDEYZ6NLA4O1EIACT
DIDECYLDIMONIUM CHLORIDEJXN40O9Y9BIACT
PHENOXYETHANOLHIE492ZZ3TIACT
IODOPROPYNYL BUTYLCARBAMATE603P14DHEBIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 3 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
DMDM HYDANTOINDMDM HYDANTOINBYR0546TOWLOTION / TOPICAL3 mgExact identifier — unii candidate
LAURAMINE OXIDELAURAMINE OXIDE4F6FC4MI8WSPONGE / TOPICALNAExact identifier — unii candidate
2 equally ranked IID candidates
LAURAMINE OXIDELAURAMINE OXIDE4F6FC4MI8WSOLUTION / TOPICAL3.5 %w/vExact identifier — unii candidate
2 equally ranked IID candidates

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
b4644afc-498c-5e01-e053-2995a90a34851bd42afd-4ac2-4a05-86cc-b65f399a85b22020-11-18WarningsExact identifier
spl id: b4644afc-498c-5e01-e053-2995a90a3485
spl set id: 1bd42afd-4ac2-4a05-86cc-b65f399a85b2

Reported adverse events (FAERS/openFDA)#

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