DrugCite

INSTANTFOAM NON-ALCOHOL  - benzalkonium chloride liquid 
PARAGON AERO INSTANT  - benzalkonium chloride liquid 
HY5 SOAPOPULAR AERO  - benzalkonium chloride liquid 
Deb USA, Inc.

Drug Facts

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

container label



INSTANTFOAM NON-ALCOHOL 
benzalkonium chloride  liquid
Product Information
Product Type HUMAN OTC DRUG NDC Product Code (Source) 11084-058
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE 0.13 mL  in 100 mL
Inactive Ingredients
Ingredient Name Strength
WATER  
PROPYLENE GLYCOL  
ALOE VERA LEAF  
COCAMIDOPROPYL BETAINE  
LAURAMINE OXIDE  
EDETATE SODIUM  
METHYLCHLOROISOTHIAZOLINONE  
METHYLISOTHIAZOLINONE  
MAGNESIUM NITRATE  
MAGNESIUM CHLORIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 11084-058-01 47 mL In 1 BOTTLE, PUMP None
2 11084-058-05 3780 mL In 1 BOTTLE, PLASTIC None
3 11084-058-12 1200 mL In 1 BOTTLE, PLASTIC None
4 11084-058-20 2000 mL In 1 BOTTLE, PLASTIC None
5 11084-058-27 1000 mL In 1 BOTTLE, PLASTIC None
6 11084-058-40 400 mL In 1 BOTTLE, PUMP None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333A 01/01/2023

PARAGON AERO INSTANT 
benzalkonium chloride  liquid
Product Information
Product Type HUMAN OTC DRUG NDC Product Code (Source) 11084-137
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE 0.13 mL  in 100 mL
Inactive Ingredients
Ingredient Name Strength
WATER  
PROPYLENE GLYCOL  
ALOE VERA LEAF  
COCAMIDOPROPYL BETAINE  
LAURAMINE OXIDE  
EDETATE SODIUM  
METHYLCHLOROISOTHIAZOLINONE  
METHYLISOTHIAZOLINONE  
MAGNESIUM NITRATE  
MAGNESIUM CHLORIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 11084-137-27 1000 mL In 1 BOTTLE, PLASTIC None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333A 01/01/2023

HY5 SOAPOPULAR AERO 
benzalkonium chloride  liquid
Product Information
Product Type HUMAN OTC DRUG NDC Product Code (Source) 11084-136
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE 0.13 mL  in 100 mL
Inactive Ingredients
Ingredient Name Strength
WATER  
PROPYLENE GLYCOL  
ALOE VERA LEAF  
COCAMIDOPROPYL BETAINE  
LAURAMINE OXIDE  
EDETATE SODIUM  
METHYLCHLOROISOTHIAZOLINONE  
METHYLISOTHIAZOLINONE  
MAGNESIUM NITRATE  
MAGNESIUM CHLORIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 11084-136-27 1000 mL In 1 BOTTLE, PLASTIC None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333A 01/01/2023

Labeler - Deb USA, Inc. (607378015)
Establishment
Name Address ID/FEI Operations
Deb USA, Inc. 607378015 manufacture
Revised: 09/2010Deb USA, Inc.