Otc - Active Ingredient
Acitive ingredient
Benzalkonium Chloride, 0.13%
Appeal Non-alcohol Foaming Hand Sanitizer
FDA Label NDC 11084-106
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Deb Usa, Inc. for the product Appeal Non-alcohol Foaming Hand Sanitizer (NDC 11084-106). 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 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
Inactive ingredients
Water, Propylene Glycol, Aloe Barbadensis Leaf Juice, Cocamidopropyl Betaine, Lauramine Oxide, Tetrasodium EDTA, Magnesium Nitrate, Methylchloroisothiazolinone, Magnesium Chloride, Methylisothiazolinone
Package Label.Principal Display Panel
APP17103
appeal
Non-alcohol Foaming Hand Sanitizer
1 Liter
33.8 Fluid Ounces
Made in the USA by Deb
deb foam technology
Distributed exclusively by:
AmSan
America's Leading Supplier of Janitorial and Cleaning Products
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