Otc - Active Ingredient
Active Ingredient Purpose
Ethanol 70% v/v........Antiseptic
Workforce Hand Sanitizer
FDA Label NDC 81122-233
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Magnus Procurement & Logistics Solution, Inc. for the product Workforce Hand Sanitizer (NDC 81122-233). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding otc - active ingredient, warnings, otc - when using, otc - keep out of reach of children, inactive ingredient, otc - purpose, otc - stop use, indications & usage, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Warnings
Warnings
For external use only. Flammable. Keep away from heat or flame.
Otc - When Using
When using this product
Avoid contact with eyes. In case of eye contact, flush eyes with water.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Inactive Ingredient
Inactive Ingredients
Water, Glycerin, Polyacrylic Acid, Frangrance.
Otc - Purpose
Antiseptic, Hand Sanitizer
Otc - Stop Use
Stop use and ask a doctor if irritation or redness develops and conditions persist for more than 72 hours.
Indications & Usage
Uses: For hand sanitizing to decrease bacteria on the skin.
Dosage & Administration
Directions
Place enough product in your palm to thoroughly cover hands. Rub thoroughly over all surfaces of both hands. Rub hands together briskly until dry.
Package Label.Principal Display Panel
1.25L Front 81122-133-25
1.25L Back 81122-133-25
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1 Gl Label (Ma1227133(wf20001 Wf20021) Hand Sanitizer Gel Ms 1 Gal Label)
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