FDA Label for United Labs Instant Foam
View Indications, Usage & Precautions
United Labs Instant Foam 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
Benzalkonium Chloride, 0.13%
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
Inactive ingredients
Water, Propylene Glycol, Aloe Barbadensis Leaf Juice, Cocamidopropyl Betaine, Lauramine Oxide, Tetrasodium EDTA, Fragrance, Citric Acid, Magnesium Nitrate, Methylchloroisothiazolinone, Magnesium Chloride, Methylisothiazolinone, Blue 1 (CI 42090), Red 33 (CI 17200)
Package Label.Principal Display Panel
deb
InstantFOAM
non-alcohol hand sanitizer
refreshing
no water required
use anywhere, any time
use everyday
Kills 99.99% of common germs
deb foam technology
56827-01-116
1 Liter - 33.8 Fluid Ounces
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