INSTANTFOAM ALCOHOL HAND SANITIZER- ethyl alcohol liquid

InstantFOAM alcohol hand sanitizer by

Drug Labeling and Warnings

InstantFOAM alcohol hand sanitizer by is a Otc medication manufactured, distributed, or labeled by Deb USA, Inc., Deb Worldwide Healthcare Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient                                                          

Ethyl Alcohol 72%

PURPOSE

Purpose

Antibacterial

INDICATIONS & USAGE

Uses

For hand sanitizing to reduce bacteria on skin

WARNINGS

Warnings

For external use only

Avoid contact with eyes

Flammable

Keep away from flame or fire

Keep out of reach of children.

Consult physician or poison control if ingested.

DOSAGE & ADMINISTRATION

Directions

Apply one shot to dry hands

Rub into skin

No rinsing required

INACTIVE INGREDIENT

Inactive Ingredients

Water, n-Propanol, Cocoglucoside, Glyceryl Oleate, PEG-7 Glyceryl Cocoate, PEG-200 Hydrogenated Glyceryl Palmate, Dihydroxypropyl PEG-5 Linoleammonium Chloride, Behentrimonium Chloride, Bis-PEG-12 Dimethicone

PRINCIPAL DISPLAY PANEL

deb

Instant Foam

alcohol hand sanitizer

refreshing

no water required

use anywhere, any time

use everyday

Kills>99.9999%

of common germs in 15 seconds

Made in Canada

Worldwide Patent Pending

deb foam technology

NSF

Nonfood Compounds Program Listed E-3 140062

01827-01-116

1 Liter - 33.8 Fluid Ounces

INGREDIENTS AND APPEARANCE

INSTANTFOAM ALCOHOL HAND SANITIZER 
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11084-017
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M)	Alcohol	72 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1)
Propyl Alcohol (UNII: 96F264O9SV)
Behentrimonium Chloride (UNII: X7GNG3S47T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11084-017-01	47 mL in 1 BOTTLE, PUMP
2	NDC: 11084-017-40	400 mL in 1 BOTTLE, SPRAY
3	NDC: 11084-017-27	1000 mL in 1 BOTTLE, SPRAY

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333	06/02/2008

Labeler - Deb USA, Inc. (607378015)

Establishment
Name	Address	ID/FEI	Business Operations
Deb Worldwide Healthcare Inc.		205662831	manufacture