Home – InstantFOAM non-alcohol

InstantFOAM non-alcohol

Deb USA, Inc.

Drug Facts

FULL PRESCRIBING INFORMATION

Active ingredient

Benzalkonium Chloride, 0.13%

Purpose

Antibacterial

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, Magnesium Nitrate, Methylchloroisothiazolinone, Mangnesium Chloride, Methylisothiazolinone

deb

InstantFOAM

non-alcohol-dye and fragrance free

hand sanitizer

refreshing

no water required

use anywhere, anytime

use everyday

Kills 99.99% of common germs

deb foam technology

NSF

Nonfood Compounds Program Listed E-3 140059

55854-01-116

1 Liter - 33.8 Fluid Ounces

InstantFOAM non-alcohol

BENZALKONIUM CHLORIDE LIQUID

Product Information
Product Type	Human otc drug label	Item Code (Source)	NDC:11084-058
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
benzalkonium chloride		0.13 mL

Inactive Ingredients
Ingredient Name	Strength
water
propylene glycol
Aloe Vera Leaf
COCAMIDOPROPYL BETAINE
LAURAMINE OXIDE
EDETATE SODIUM
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE
MAGNESIUM NITRATE
MAGNESIUM CHLORIDE

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC:11084-058-01	47 in 1 BOTTLE, PUMP
2	NDC:11084-058-05	3780 in 1 BOTTLE, PLASTIC
3	NDC:11084-058-12	1200 in 1 BOTTLE, PLASTIC
4	NDC:11084-058-20	2000 in 1 BOTTLE, PLASTIC
5	NDC:11084-058-27	1000 in 1 BOTTLE, PLASTIC
6	NDC:11084-058-40	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

Paragon Aero Instant

Benzalkonium Chloride LIQUID

Product Information
Product Type	Human otc drug label	Item Code (Source)	NDC:11084-137
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
benzalkonium chloride		0.13 mL

Inactive Ingredients
Ingredient Name	Strength
water
propylene glycol
Aloe Vera Leaf
COCAMIDOPROPYL BETAINE
LAURAMINE OXIDE
EDETATE SODIUM
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE
MAGNESIUM NITRATE
MAGNESIUM CHLORIDE

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC:11084-137-27	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

Hy5 Soapopular Aero

Benzalkonium Chloride LIQUID

Product Information
Product Type	Human otc drug label	Item Code (Source)	NDC:11084-136
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
benzalkonium chloride		0.13 mL

Inactive Ingredients
Ingredient Name	Strength
water
propylene glycol
Aloe Vera Leaf
COCAMIDOPROPYL BETAINE
LAURAMINE OXIDE
EDETATE SODIUM
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE
MAGNESIUM NITRATE
MAGNESIUM CHLORIDE

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC:11084-136-27	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

PLEASE, BE CAREFUL!

Be sure to consult your doctor before taking any medication!