FDA Label for Instantfoam Alcohol Hand Sanitizer
View Indications, Usage & Precautions
Instantfoam Alcohol Hand Sanitizer Product Label
The following document was submitted to the FDA by the labeler of this product Deb Usa, Inc.. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Otc - Active Ingredient
Active Ingredient
Ethyl Alcohol 72%
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
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