AIR CANADA FOAM HAND SANITIZER- benzalkonium chloride liquid 
Freshorize 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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Air Canada Alcohol Free Foam Hand Sanitizer

Uses:

To decrease bacteria on the skin.

Warnings:


For external use only. Keep out of reach of children. Avoid contact with
eyes. In case of contact, rinse eyes thoroughly with water. Stop use and ask a
doctor if skin irritation develops. If ingested, seek medical help or contact a Poison
Control Centre immediately.

Warnings:

Keep out of reach of children.

Directions:


Apply a small amount on the hands and rub lightly until dry.
Supervise children in the use of the product.

Directions:

Apply a small amount on the hands and rub lightly until dry.

Other information:

Avoid extreme temperatures.

Inactive Ingredients:


Aqua, Glycerin, PEG-40 Hydrogenated Castor Oil,
Propylene Glycol, Parfum, DMDM Hydantoin, Aloe Barbadensis Leaf Extract.

Drug Facts:

Active Ingredient: Benzalkonium Chloride

Drug Facts

Purpose: Antibacterial

Air Canada Label

AIR CANADA FOAM HAND SANITIZER 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52305-603
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
DMDM HYDANTOIN (UNII: BYR0546TOW) 0.2 g  in 100 mL
PROPYLENE (UNII: AUG1H506LY) 0.5 g  in 100 mL
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY) 0.75 g  in 100 mL
ALOE VERA LEAF (UNII: ZY81Z83H0X) 0.1 g  in 100 mL
GLYCERIN (UNII: PDC6A3C0OX) 3 g  in 100 mL
WATER (UNII: 059QF0KO0R) 95.07 g  in 100 mL
Product Characteristics
Color    Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52305-603-24240 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product12/04/2020
Image of Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A12/04/2020
Labeler - Freshorize Ltd (424168503)
Registrant - Freshorize LLC (018206924)
Establishment
NameAddressID/FEIBusiness Operations
China Ningbo Shangge Cosmetic Technology Corp529287434manufacture(52305-603)

Revised: 12/2020
Document Id: b5a621c1-ea18-f533-e053-2a95a90a541a
Set id: b5a621c1-ea17-f533-e053-2a95a90a541a
Version: 1
Effective Time: 20201204
 
Freshorize Ltd