Otc - Active Ingredient
Active ingredient
Benzalkonium Chloride, 0.13%
Proformance Series Foam Non-alcohol Sanitizer
FDA Label NDC 66908-106
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Pro-link, Inc. for the product Proformance Series Foam Non-alcohol Sanitizer (NDC 66908-106). 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, indications & usage, warnings, otc - when using, 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
Otc - Purpose
Purpose
Antibacterial
Indications & Usage
Uses
For hand sanitizing to reduce bacteria on the skin
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 - 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.
Dosage & Administration
Directions
Apply one shot to dry hands, rub into skin
No rinsing required
Inactive Ingredient
Water, Propylene Glycol, Aloe Barbadensis Leaf Juice, Cocamidopropyl Betaine, Lauramine Oxide, Tetrasodium EDTA, Magnesium Nitrate, Methylchloroisothiazolinone, Magnesium Chloride, Methylisothiazolinone.
Package Label.Principal Display Panel
ProFormance Series
Foam Non-Alcohol Sanitizer
Pro-Link
MSN1000
Distributed exclusively by
Pro-Link, Inc.
1 Liter
33.8 Fluid Ounces
* Please review the disclaimer below.
