FDA.reportPublic FDA data

Workforce Foaming Hand Sanitizer E3

Manufacturer
Magnus Procurement & Logistics Solution, Inc. | Seatex, LLC
Effective date
2021-12-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:22:39

Label at a glance#

ProductWorkforce Foaming Hand Sanitizer E3
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient Purpose

Benzalkonium Chloride 0.1%...................Antimicrobial

INDICATIONS & USAGE SECTION

Uses

For hand sanitizing to decrease bacteria on the skin.

Recommended for repeated use.

OTC - WHEN USING SECTION

When using this product Avoid contact with eyes. In case of eye contact, flush eyes with water. Do not ingest.

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.

DOSAGE & ADMINISTRATION SECTION

Directions

Pump a small amount of foam into palm of hand.

Rub thoroughly over all surffaces of both hands

Rub hands together briskly until dry.

INACTIVE INGREDIENT SECTION

Inactive Ingredients

Water, Cetrimonium Chloride, Laurtrimonium Chloride, Dihydroxyethyl Cocamine Oxide

OTC - STOP USE SECTION

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

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

WARNINGS SECTION

Warnings For External use only.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1 gl label1 gl label3.785 L 81122-120-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1.25 L Front Label1.25 L Front Label1.25 L 81122-120-50

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1.25 L Back Label1.25 L Back Label1.25 L 81122-120-50

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81122-12081122-120-01, 81122-120-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
LAURTRIMONIUM CHLORIDEA81MSI0FICIACT
DIHYDROXYETHYL COCAMINE OXIDE8AR51R3BL5IACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
d2a90883-3e29-bac9-e053-2a95a90a92deb467dce9-3d45-b819-e053-2995a90a60fc2021-12-08WarningsExact identifier
spl id: d2a90883-3e29-bac9-e053-2a95a90a92de
spl set id: b467dce9-3d45-b819-e053-2995a90a60fc

Reported adverse events (FAERS/openFDA)#

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