Workforce

Manufacturer
Magnus Procurement & Logistics Solution, Inc. | SeaTex, LLC
Effective date
2022-09-19
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 21:53:27

Label at a glance#

ProductWorkforce
Active ingredientBENZALKONIUM CHLORIDE
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient Purpose

Benzalkonium Chloride 0.13%............Antibacterial

INDICATIONS & USAGE SECTION

Uses

For hand washing to decrease bacteria on the skin.

WARNINGS SECTION

Warnings For external use only.

OTC - WHEN USING SECTION

When using this product Avoid contact with eyes. In case of eye contact, flush eyes with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develops. or if condition persists 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 Contdrol Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions

Pump into hands, wet as needed.

Lather vigorously for at least 15 seconds.

Wash skin, rinse thoroughly and dry.

INACTIVE INGREDIENT SECTION

Inactive Ingredients

Water, Laurtrimonium Chloride, Alkyl Polyglucoside, Citric Acid, Dye, Fragrance.

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1.25 L Front Label1.25 L Front Label1.25 L 81122-101-25

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1.25 L Back label1.25 L Back label1.25 L 81122-101-25

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81122-10181122-101-25

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

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
e90f4c08-0de8-f73e-e053-2a95a90a7faab3d94a86-d00c-072e-e053-2a95a90acf692022-09-19WarningsExact identifier
spl id: e90f4c08-0de8-f73e-e053-2a95a90a7faa
spl set id: b3d94a86-d00c-072e-e053-2a95a90acf69

Reported adverse events (FAERS/openFDA)#

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