Otc - Active Ingredient
Benzalkonium chloride 0.1%
Hygenix Af Gel
FDA Label NDC 74146-244
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Gm Industrial, Inc. for the product Hygenix Af Gel (NDC 74146-244). 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, otc - purpose, uses, 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
Otc - Purpose
Antimicrobial
Uses
For hand sanitizing to decrease bacteria on the skin.
Recommended for repeated use.
Warnings
For external use only
Otc - When Using
When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.
Otc - Stop Use
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
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- Pump a small amount of gel into pal of hand
- Rub thoroughly over all surfaces of both hands
- Rub hands together briskly until dry.
Inactive Ingredient
Water, carbomer, glycerin, lactic acid.
Package Label.Principal Display Panel
74146-244-02
200 mL Ndc: 74146-244-02 (L23494 Bn2c Zenex)
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