INSTANTFOAM NON-ALCOHOL  - benzalkonium chloride liquid 
Deb USA, Inc.

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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

INSTANTFOAM NON-ALCOHOL  benzalkonium chloride, 0.13%   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	01/01/2010

Labeler - Deb USA, Inc. (607378015)

Establishment
Name	Address	ID/FEI	Operations
Deb USA, Inc.		607378015	manufacture

Revised: 09/2010Deb USA, Inc.