FOAMING HAND SANITIZER- alcohol solution 
Empack Spraytech 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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Active Ingredient(s)

Ethanol 70% (v/v)

Purpose

Antiseptic

Uses

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

For external use only. Flammability warning. Keep away from open flame and sources of heat.

Do not use

When using this product, avoid contact with eyes. If contact occurs, rinse thoroughly with water. 

Stop use and ask a doctor if irritation develops.

Keep out of reach of children. Topical. If swallowed, call a poison control centre or get medical help right away.

Directions

Other information

Inactive ingredients

Water, Bis-PEG-12 Dimethicone, Glycerin, Aloe Barbadensis Leaf Juice

Questions?

1-866-923-2665

UPC

Manufactured by Empack Spraytech Inc., 98 Walker Drive, Brampton, ON, Canada L6T 4H6

www.zytecgermbuster.ca

Made in Canada

Lot # and Expiry Date to be embossed on the bottle

Package Label - Principal Display Panel

550 ml; NDC 50021-020-01Foaming Hand Sanitizer

FOAMING HAND SANITIZER 
alcohol solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50021-020
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
GLYCERIN (UNII: PDC6A3C0OX)  
BIS-PEG-12 DIMETHICONE (500 MPA.S) (UNII: 2CNS542YRT)  
WATER (UNII: 059QF0KO0R)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:50021-020-01550 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product11/11/2020
2NDC:50021-020-023785 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product11/11/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A11/11/2020
Labeler - Empack Spraytech Inc. (252047519)
Registrant - Empack Spraytech Inc. (252047519)
Establishment
NameAddressID/FEIBusiness Operations
Empack Spraytech Inc.252047519manufacture(50021-020)

Revised: 11/2020
Document Id: c4299b0c-94ab-4d29-b7f8-70381966c41c
Set id: 8bb072f2-9cd4-499d-9d7f-7166451b8f20
Version: 1
Effective Time: 20201111
 
Empack Spraytech Inc.