ECO SANITIZER GEL- ethyl alcohol gel 
0966452 B.C. Ltd.

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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eco SANITIZER HAND SANITIZER GEL

Purpose: Antiseptic

Use: Hand sanitizer to help reduce bacteria on skin

Directions for Use: Supervise children when they use this product. For occasional and personal domestic use. Rub thoroughly into hands for at least 30 seconds. Allow to dry.

Medicinal Ingredients: Ethyl Alcohol* (70% v/v).

Ingredients: Aqua, Glycerin,* Hydroxypropylcellulose*. *Plant based ingredient.

Warning: For external use only. Keep out of reach of children. Flammable. Keep away from open flame and sources of heat. Avoid contact with eyes. Should this occur, flush eyes with water. If irritation develops, discontinue use and contact a health care practitioner. Store between 15°C/59°F and 30°C/86°F.

Contraindications: Do not use on children/infants less than 2 years of age (unless directed by a health care practitioner).

Keep out of reach of children.

kills 99% of germs

Get your hands on it!

Fragrance free | Hypoallergenic

Enriched Gel with Glycerin | Can be used as is or as a refill

Made in Canada from Domestic and Imported products.

Eco Sanitizer | ecosanitizer.ca

Packaging

IMAGE

ECO SANITIZER GEL 
ethyl alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80731-002
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:80731-002-0150 mL in 1 BOTTLE; Type 0: Not a Combination Product10/08/2020
2NDC:80731-002-05320 mL in 1 BOTTLE; Type 0: Not a Combination Product10/27/2020
3NDC:80731-002-031000 mL in 1 BOTTLE; Type 0: Not a Combination Product10/08/2020
4NDC:80731-002-044000 mL in 1 BOTTLE; Type 0: Not a Combination Product10/08/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A10/08/2020
Labeler - 0966452 B.C. Ltd. (204193445)
Establishment
NameAddressID/FEIBusiness Operations
0966452 B.C. Ltd.204193445manufacture(80731-002)

Revised: 10/2020
Document Id: 6bf30eb9-f002-45bd-bd21-4a9b4edf637b
Set id: 352f17a9-7a53-459d-b367-6796cf1a01c2
Version: 2
Effective Time: 20201028
 
0966452 B.C. Ltd.