FDA.reportPublic FDA data

United Airlines

Manufacturer
Freshorize Ltd | Freshorize LLC | China Ningbo Shangge Cosmetic Technology Corp.
Effective date
2025-10-23
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-06-01 01:40:28

Label at a glance#

ProductUnited Airlines
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

To decrease bacteria on skin.

Dosage and administration

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

Label contents#

Full prescribing information#

Uses:

INDICATIONS & USAGE SECTION

To decrease bacteria on skin.

Warnings:

WARNINGS SECTION

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:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

INSTRUCTIONS FOR USE SECTION

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

Other Information:

OTHER SAFETY INFORMATION

Avoid extreme temperatures.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

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

Drug Facts:

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Benzalkonium Chloride 0.13%

Purpose:

OTC - PURPOSE SECTION

Antibacterial.

Product / Brand Name Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Front Label

DOSAGE & ADMINISTRATION SECTION

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

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1049254benzalkonium chloride 0.13 % Topical SolutionPSN7
1049254benzalkonium chloride 1.3 MG/ML Topical SolutionSCD7
1049254benzalkonium chloride 0.13 % Topical SolutionSY7

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52305-601-25United Airlines250 mL in 1 BOTTLE, PUMPLIQUID2507

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52305-60152305-601-25

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
HYDROGENATED CASTOR OILZF94AP8MEYIACT
PROPYLENEAUG1H506LYIACT
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT
GLYCERINPDC6A3C0OXIACT
DMDM HYDANTOINBYR0546TOWIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
62024-10-17full-release2026-06-01 00:27:10

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
United AirlinesBENZALKONIUM CHLORIDEFreshorize Ltda8d96b43-272a-9e49-e053-2995a90a3cc12025-10-23WarningsExact identifier
ndc (package): 52305-601-25
ndc (product): 52305-601
ndc11 (package): 52305060125
spl id: 41d6d63a-3546-673f-e063-6394a90a5c3f
spl set id: a8d96b43-272a-9e49-e053-2995a90a3cc1

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.