FDA.reportPublic FDA data

Alaska Airlines

Manufacturer
Freshorize Ltd. | Freshorize LLC | China Ningbo Shangge Cosmetic Technology Corp.
Effective date
2025-10-23
Label type
HUMAN OTC DRUG LABEL
Version
9
Source
full-release
Hydrated at
2026-06-01 01:40:28

Label at a glance#

ProductAlaska Airlines
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

To decrease bacteria on the 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#

Warnings:

WARNINGS SECTION

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:

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.

Uses:

INDICATIONS & USAGE SECTION

To decrease bacteria on the skin.

Purpose:

OTC - PURPOSE SECTION

Antibacterial.

Drug facts:

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Benzalkonium Chloride.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

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

Other Information:

OTHER SAFETY INFORMATION

Avoid extreme temperatures.

Alaska Arilines Foam Hand Sanitizer

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Alaska Alcohol Free Hand SanitizerAlaska Alcohol Free Hand Sanitizer

Alaska hand Sanitizer

DOSAGE & ADMINISTRATION SECTION

Hand Sanitizer
Ocean Citron

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

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1049254benzalkonium chloride 0.13 % Topical SolutionPSN9
1049254benzalkonium chloride 1.3 MG/ML Topical SolutionSCD9
1049254benzalkonium chloride 0.13 % Topical SolutionSY9

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52305-602-30Alaska Airlines250 mL in 1 BOTTLE, PUMPLIQUID2509

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
52305-60252305-602-30

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
PROPYLENEAUG1H506LYIACT
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT
DMDM HYDANTOINBYR0546TOWIACT
GLYCERINPDC6A3C0OXIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
82024-10-17full-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
Alaska AirlinesBENZALKONIUM CHLORIDEFreshorize Ltd.a8ed793e-988e-d815-e053-2995a90a3d312025-10-23WarningsExact identifier
ndc (package): 52305-602-30
ndc (product): 52305-602
ndc11 (package): 52305060230
spl id: 41d6f1f9-65bd-24f4-e063-6294a90a51a1
spl set id: a8ed793e-988e-d815-e053-2995a90a3d31

Reported adverse events (FAERS/openFDA)#

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