Otc - Active Ingredient
Active ingredient
Benzalkonium Chloride 0.13%
Dermacen Non-alcohol Foaming Hand Sanitizer Solution
FDA Label NDC 62654-141
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Central Solutions Inc for the product Dermacen Non-alcohol Foaming Hand Sanitizer (NDC 62654-141). 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, indications & usage, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, dosage & administration, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Indications & Usage
Uses
For hand sanitizing to decrease bacteria on the skin
Recommended for repeated use
Warnings
Warnings
For external use only
Otc - When Using
When using this product avoid contact with eyes.
In case of eye contact, flush with water.
Otc - Stop Use
Stop use and ask a doctor if irritation or redness develops, or if conditions persists for more than 72 hours.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, call a physician or Poison Control Center right away.
Dosage & Administration
Directions
Pump a small amount of foam into palm of hand
Rub thoroughly over all surfaces of both hands
Rub hands together briskly until dry
Inactive Ingredient
Inactive ingredients
Purified Water, Glycerin, Cocamidopropyl Betaine, Triethanolamine
Otc - Purpose
Purpose
Hand Sanitizer
Package Label.Principal Display Panel
DermaCen
Non-Alcohol
Foaming Instant
Hand Sanitizer
For hand sanitizing
to decrease bacteria
on the skin
NET CONTENTS: 18 ounces (532 mL)
* Please review the disclaimer below.
