FDA.reportPublic FDA data

Workforce Hand Sanitizer Gel

Manufacturer
Magnus Procurement & Logistics Solution, Inc. | Seatex, LLC
Effective date
2021-12-10
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 22:23:13

Label at a glance#

ProductWorkforce Hand Sanitizer Gel
Active ingredientISOPROPYL ALCOHOL
Label structure13 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient Purpose

Isopropyl Alcohol 70% v/v..........Antiseptic

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

INDICATIONS & USAGE SECTION

Uses

For hand sanitizing to decrease bacteria on the skin.

WARNINGS SECTION

Warnings For external use only.

Flammable. Keep away from heat or flame.

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 and conditions persist 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.

DOSAGE & ADMINISTRATION SECTION

Directions

Place enough product in your palm to

thoroughly cover hands

Rub hands together briskly until dry.

Children under 6 years of age shoud be

supervised when using this product.

INACTIVE INGREDIENT SECTION

Inactive Ingredients

Polyacrylic Acid, Water, Dye

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1gl 81122-134-01 label1gl 81122-134-01 label1 gl 81122-134-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

16 oz label16 oz label16 oz 81122-134-16

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1.25 L Front Label1.25 L Front Label1.25 L 81122-134-25

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1.25 L Back Label1.25 L Back Label1.25 L back 81122-134-25

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81122-13481122-134-01, 81122-134-25, 81122-134-16

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
ISOPROPYL ALCOHOLND2M416302ACTIB
RAPIDGEL EZ133JH4A7R2KIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
FD&C YELLOW NO. 5I753WB2F1MIACT

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
d2ceffdb-325c-40e0-e053-2a95a90a8f13b467fa1b-93a4-9233-e053-2a95a90a31d92021-12-10WarningsExact identifier
spl id: d2ceffdb-325c-40e0-e053-2a95a90a8f13
spl set id: b467fa1b-93a4-9233-e053-2a95a90a31d9

Reported adverse events (FAERS/openFDA)#

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