UNITED AIRLINES- benzalkonium chloride liquid

United Airlines by

Drug Labeling and Warnings

United 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]

Uses:

To decrease bacteria on skin.

Warnings:

For external use only.
Do not use in eyes.
In cse of contact, rinse eyes thoroughly with water.
Stop use and ask a doctor is 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.

Other Information:

Avoid extreme temperatures.

Inactive Ingredients:

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

Drug Facts:

Active Ingredients: Benzalkonium Chloride 0.13%

Purpose:

Antibacterial.

Product / Brand Name Label

Front Label

This product is a hand sanitizer liquid pump. There is no dosage. But typically a passenger will use 1-2 pumps.

INGREDIENTS AND APPEARANCE

UNITED AIRLINES 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52305-601
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
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)	0.75 g  in 100 mL
PROPYLENE (UNII: AUG1H506LY)	0.5 g  in 100 mL
WATER (UNII: 059QF0KO0R)	95.07 g  in 100 mL
ALOE VERA LEAF (UNII: ZY81Z83H0X)	0.1 g  in 100 mL
GLYCERIN (UNII: PDC6A3C0OX)	3 g  in 100 mL
DMDM HYDANTOIN (UNII: BYR0546TOW)	0.2 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: 52305-601-25	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(52305-601)