CLEAN CHOICE ALCOHOL SANITIZER- 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.

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Drug Facts

Active ingredient

Ethyl Alcohol 70% ww

Purpose

Antibacterial

Uses

For hand sanitizing to reduce bacteria on the skin

Warnings

For external use only

Flammable: Keep away from fire or flame.

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 foaming sanitizer to cover hands

Rub into skin

No rinsing required

Inactive ingredients

Water, Bis-PEG-12 Dimethicone, Behentrimonium Chloride, PEG-200 Hydrogenated Glyceryl Palmate, PEG-7 Glyceryl Cocoate, Coco-Glucoside, Glyceryl Oleate, Dihydroxypropyl PEG-5 Linoleammonium Chlroide.

Clean Choice Foaming Alcohol Hand Sanitizer

Certified Ecologo

Certified NSF Instant Hand Antiseptic CCD-170

USDA Certified Biobased Product

1 Liter

33.8 fl. oz.

Part #0617381

Distributed by Fastenal Co.

Winona, MN 55987

2013 fastenal.com

Made in Canada

0617381

Alcohol Hand Sanitizer

Rev. 08-13-116

product label front

product label back

CLEAN CHOICE ALCOHOL SANITIZER 
ethyl alcohol liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:11084-704
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M) Alcohol 70 L  in 100 L
Inactive Ingredients
Ingredient Name Strength
WATER (UNII: 059QF0KO0R)  
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1)  
BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
COCO GLUCOSIDE (UNII: ICS790225B)  
PEG-200 DILAURATE (UNII: TWV5J70L88)  
GLYCERYL COCOATE (UNII: WVK1CT5994)  
GLYCERYL MONOOLEATE (UNII: 4PC054V79P)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:11084-704-27 1 L in 1 BOTTLE, PLASTIC
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333E 09/15/2013
Labeler - Deb USA, Inc. (607378015)
Establishment
Name Address ID/FEI Business Operations
Deb Worldwide Healthcare Inc. 205662831 manufacture(11084-704)

Revised: 9/2013
Document Id: 9903a162-359e-4d12-9637-4695c8eaf46d
Set id: 481b554c-6f6a-494c-88a1-78d143059c70
Version: 1
Effective Time: 20130912
 
Deb USA, Inc.