Deb USA, Inc.
Drug Facts
FULL PRESCRIBING INFORMATION
Active ingredient
Active ingredient
Benzalkonium Chloride, 0.13%
Purpose
Purpose
Antibacterial
Uses
Uses
For hand sanitizing to reduce bacteria on the skin
Warnings
For external use only
When using this product avoid contact with eyes.
In case of eye contact, flush with water.
Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Apply one shot to dry hands, rub into skin
No rinsing required
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)
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
InstantFOAM non-alcohol hand sanitizer
Benzalkonium Chloride LIQUID
Product Information
|
Product Type
|
Human otc drug label |
Item Code (Source)
|
NDC:11084-057 |
Route of Administration
|
TOPICAL |
DEA Schedule
|
|
Packaging
|
#
|
Item Code
|
Package Description
|
Marketing Start Date
|
Marketing End Date
|
1 |
NDC:11084-057-01 |
47 in 1 BOTTLE, PUMP |
|
|
2 |
NDC:11084-057-05 |
3780 in 1 BOTTLE, PLASTIC |
|
|
3 |
NDC:11084-057-20 |
2000 in 1 BOTTLE, PLASTIC |
|
|
4 |
NDC:11084-057-27 |
1000 in 1 BOTTLE, PLASTIC |
|
|
5 |
NDC:11084-057-40 |
400 in 1 BOTTLE, PUMP |
|
|
Marketing Information
|
Marketing Category
|
Application Number or Monograph Citation
|
Marketing Start Date
|
Marketing End Date
|
partA |
part333A |
2010-01-01 |
|
|
Safe-T-Fresh Alcohol Free Hand Sanitizer
Benzalkonium Chloride LIQUID
Product Information
|
Product Type
|
Human otc drug label |
Item Code (Source)
|
NDC:11084-129 |
Route of Administration
|
TOPICAL |
DEA Schedule
|
|
Packaging
|
#
|
Item Code
|
Package Description
|
Marketing Start Date
|
Marketing End Date
|
1 |
NDC:11084-129-27 |
1000 in 1 BOTTLE, PLASTIC |
|
|
Marketing Information
|
Marketing Category
|
Application Number or Monograph Citation
|
Marketing Start Date
|
Marketing End Date
|
partA |
part333A |
2010-01-01 |
|
|
Drummond Aero Instant
Benzalkonium Chloride LIQUID
Product Information
|
Product Type
|
Human otc drug label |
Item Code (Source)
|
NDC:11084-112 |
Route of Administration
|
TOPICAL |
DEA Schedule
|
|
Packaging
|
#
|
Item Code
|
Package Description
|
Marketing Start Date
|
Marketing End Date
|
1 |
NDC:11084-112-01 |
47 in 1 BOTTLE, PUMP |
|
|
2 |
NDC:11084-112-27 |
1000 in 1 BOTTLE, PLASTIC |
|
|
Marketing Information
|
Marketing Category
|
Application Number or Monograph Citation
|
Marketing Start Date
|
Marketing End Date
|
partA |
part333A |
2010-01-01 |
|
|
United Labs Instant Foam
Benzalkonium Chloride LIQUID
Product Information
|
Product Type
|
Human otc drug label |
Item Code (Source)
|
NDC:11084-113 |
Route of Administration
|
TOPICAL |
DEA Schedule
|
|
Packaging
|
#
|
Item Code
|
Package Description
|
Marketing Start Date
|
Marketing End Date
|
1 |
NDC:11084-113-27 |
400 in 1 BOTTLE, PUMP |
|
|
2 |
NDC:11084-113-40 |
47 in 1 BOTTLE, PUMP |
|
|
Marketing Information
|
Marketing Category
|
Application Number or Monograph Citation
|
Marketing Start Date
|
Marketing End Date
|
partA |
part333A |
2010-01-01 |
|
|