Active Ingredient
Ethyl Alcohol 70% v/v.
Pfa Gel
FDA Label NDC 75742-008
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zhejiang Guoyao Jingyue Aerosol Co., Ltd. for the product Pfa (NDC 75742-008). 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 active ingredient, purpose, use, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antimicrobial
Use
Hand sanitizing to help reduce bacteria on the skin.
Warnings
For external use only. Flammable. Keep away from fire or flame
Otc - When Using
When using this product avoid contact with the eyes. In case of contact, flush eyes thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor if irritation and redness develops or persists.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.
Directions
- Place enough product on hands to cover hands & rub together briskly until the liquid is dry.
- Children under 6 should be supervised when using Sanitizers.
Other Information
- Store below 110F (43C)
- May discolor certain fabrics or surfaces.
Inactive Ingredients
Carbomer, Glycerin, Grapefruit seed extract, Mentha Oil, Propylene Glycol, Purified water, Sophora extract, Triethanolamine
Package Label - Principal Display Panel
60 mL/2 fl.oz
Principal Display Panel (Label 1)
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