Otc - Active Ingredient
Active Ingredient
Ethyl Alcohol 72%
Instantfoam Alcohol Hand Sanitizer
FDA Label NDC 11084-017
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 Instantfoam Alcohol Hand Sanitizer (NDC 11084-017). 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 - keep out of reach of children, dosage & administration, inactive ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
PurposeAntibacterial
Indications & Usage
Uses
For hand sanitizing to reduce bacteria on skin
Warnings
Warnings
For external use only
Avoid contact with eyes
Flammable
Keep away from flame or fire
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Consult physician or poison control if ingested.
Dosage & Administration
Directions
Apply one shot to dry hands
Rub into skin
No rinsing required
Inactive Ingredient
Inactive Ingredients
Water, n-Propanol, Cocoglucoside, Glyceryl Oleate, PEG-7 Glyceryl Cocoate, PEG-200 Hydrogenated Glyceryl Palmate, Dihydroxypropyl PEG-5 Linoleammonium Chloride, Behentrimonium Chloride, Bis-PEG-12 Dimethicone
Package Label.Principal Display Panel
deb
Instant Foam
alcohol hand sanitizer
refreshing
no water required
use anywhere, any time
use everyday
Kills>99.9999%
of common germs in 15 seconds
Made in Canada
Worldwide Patent Pending
deb foam technology
NSF
Nonfood Compounds Program Listed E-3 140062
01827-01-116
1 Liter - 33.8 Fluid Ounces
* Please review the disclaimer below.
