ALASKA AIRLINES- benzalkonium chloride liquid

Alaska Airlines by

Drug Labeling and Warnings

Alaska Airlines by is a Otc medication manufactured, distributed, or labeled by Freshorize Ltd., Freshorize LLC, China Ningbo Shangge Cosmetic Technology Corp.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Warnings:

For external use only.

Do not use in eyes. In case of contact, rinse eyes thoroughly with water.
Stop use and ask a doctor if skin irritation develops.
If ingested, get medical help or contact a Poison Control Center immediately.

Warnings:

Keep out of reach of children.

Directions:

Liberally apply product to skin by gently massaging until absorbed.
Supervise children in the use of this product.

Uses:

To decrease bacteria on the skin.

Purpose:

Antibacterial.

Drug facts:

Active Ingredients: Benzalkonium Chloride.

Inactive Ingredients:

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

Other Information:

Avoid extreme temperatures.

Alaska Arilines Foam Hand Sanitizer

Alaska hand Sanitizer

Hand Sanitizer
Ocean Citron

This is a pump item with no dosage information. Most customers use 1-2 pumps.

INGREDIENTS AND APPEARANCE

ALASKA AIRLINES 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52305-602
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
PROPYLENE (UNII: AUG1H506LY)	0.5 g  in 100 mL
WATER (UNII: 059QF0KO0R)	97.05 g  in 100 mL
ALOE VERA LEAF (UNII: ZY81Z83H0X)	0.1 g  in 100 mL
DMDM HYDANTOIN (UNII: BYR0546TOW)	0.2 g  in 100 mL
GLYCERIN (UNII: PDC6A3C0OX)	3 g  in 100 mL
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)	0.75 g  in 100 mL

Product Characteristics
Color		Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52305-602-30	250 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/29/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	06/29/2020

Labeler - Freshorize Ltd. (424168503)

Registrant - Freshorize LLC (018206924)

Establishment
Name	Address	ID/FEI	Business Operations
China Ningbo Shangge Cosmetic Technology Corp.		529287434	manufacture(52305-602)