Otc - Active Ingredient
Active ingredient
Benzalkonium Chloride, 0.13%
United Labs Instant Foam
FDA Label NDC 11084-113
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 United Labs Instant Foam (NDC 11084-113). 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 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
* Please review the disclaimer below.
