Otc - Active Ingredient
Active ingredient
Ethyl Alcohol 72%
Proformance Series Foam Alcohol Hand Sanitizer
FDA Label NDC 66908-107
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 Alcohol Hand Sanitizer (NDC 66908-107). 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 skin
Warnings
Warnings
For external use only
Flammable: Keep away from fire or flame.
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 of foaming sanitizer to dry hands
Rub into skin
No rinsing required
Inactive Ingredient
Inactive ingredients
Water, n-Propanol, Bis-PEG-12 Dimethicone, Behentrimonium Chloride, PEG-200 Hydrogenated Glyceryl Palmate, PEG-7 Glyceryl Cocoate, Coco-Glucoside, Glyceryl Oleate, Dihydroxypropyl PEG-5 Linoleammonim Chloride
Package Label.Principal Display Panel
ProFormance Series
Foam Alcohol Sanitizer
Pro-Link Green
Certified EcoLogo
Certified Instant Hand Antiseptic CCD-170
MSA1000
Distributed exclusively by:
Pro-Link, Inc.
1 Liter
33.8 Fluid Ounces
* Please review the disclaimer below.
