Boxed Warning
Drug Facts
Hygenix Af Wipe
FDA Label NDC 74146-243
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 Wipe (NDC 74146-243). 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 boxed warning, otc - active ingredient, otc - purpose, indications & usage, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Active Ingredient
Active Ingredient
Benzalkonium Chloride 0.1
Otc - Purpose
Antiseptic
Indications & Usage
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 react of children
In case of accidental ingestion, seek medical attention or contact a Poison Control Center immediately.
Dosage & Administration
Directions
Wet hands thoroughly with product.
Discard wipe in trash receptacle after use. Do not flush.
Rub hands together briskly until dry.
Other Safety Information
Other information
Store in a cool dry place below 104 °F
Inactive Ingredient
Water, C9-11 Pareth-6, Cocamidopropyl PG-dimonium chloride phosphate, Dihydroxyethyl cocamine oxide, Acetamidoethoxyethanol, Citric acid.
Package Label.Principal Display Panel
90 Ct 74146-243-93 (L480452 Ws90 Zenex Pdp)
74146-243-85
225 Ct 74146-243-85 (L480452 Ws225 Zenex Pdp)
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