INSTANTFOAM ALCOHOL HAND SANITIZER - ethyl alcohol liquid 
Deb USA, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

Drug Facts

Active Ingredient                                                          

Ethyl Alcohol 72%


Purpose

Antibacterial

Uses

For hand sanitizing to reduce bacteria on skin


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.

Directions

Apply one shot to dry hands

Rub into skin

No rinsing required


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


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

container label

INSTANTFOAM ALCOHOL HAND SANITIZER 
ethyl alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11084-017
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M) Alcohol72 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1)  
Propyl Alcohol (UNII: 96F264O9SV)  
Behentrimonium Chloride (UNII: X7GNG3S47T)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11084-017-0147 mL in 1 BOTTLE, PUMP
2NDC:11084-017-40400 mL in 1 BOTTLE, SPRAY
3NDC:11084-017-271000 mL in 1 BOTTLE, SPRAY
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33306/02/2008
Labeler - Deb USA, Inc. (607378015)
Establishment
NameAddressID/FEIBusiness Operations
Deb Worldwide Healthcare Inc.205662831manufacture

Revised: 8/2010
Document Id: 7c1bda11-b9c7-4aa1-ad2f-3a101bcdced6
Set id: 929eb8b6-0b39-4800-97b9-fc2fc910ccc7
Version: 1
Effective Time: 20100819
 
Deb USA, Inc.