Oxygen

Manufacturer
Medox Corporation
Effective date
2025-12-30
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
17
Source
full-release
Hydrated at
2026-05-31 21:53:17

Label at a glance#

ProductOxygen
Active ingredientOXYGEN
Label structure1 sections

Label contents#

Full prescribing information#

Principal for Oxygen Product

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HPLabelHPLabel

MEDOX CORPORATION

OXYGEN, COMPRESSED

USP

UN1072

PRODUCED BY AIR LIQUEFACTION

WARNING: For emergency use only when administered by properly trained personnel for oxygen deficiency and resuscitation. For all other medical applications, Rx only.

Uninterrupted use of high concentrations of oxygen over a long duration, without monitoring its effect on oxygen content of arterial blood, may be harmful. Do not attempt to use on patients who have stopped breathing unless used in conjunction with resuscitative equipment. Keep out of reach of children.

Federal law requires that this container be refilled with oxygen USP only by establishments registered as a drug manufacturer in accordance with the Federal Food, Drug, and Cosmetic Act.

DANGER: MAY CAUSE OR INTENSIFY FIRE; OXIDIZER.

CONTAINS GAS UNDER PRESSURE; MAY EXPLODE IF HEATED.

Do not handle until all safety precautions have been read and understood.

Keep and store away from clothing and other combustible materials.

Keep valves and fittings free from grease and oil.

Use and store only outdoors or in a well-ventilated place.

In case of fire: Stop leak if safe to do so.

Use a back flow preventive device in the piping.

Close valve after each use and when empty.

Use only with equipment rated for cylinder pressure.

Do not open valve until connected to equipment prepared for use.

Use only equipment of compatible materials of construction.

Open valve slowly.

Use only with equipment cleaned for oxygen service.

Protect from sunlight when ambient temperature exceeds 52°C (125°F).

Read and follow the Safety Data Sheet (SDS) before use.

OXYGEN

2

DO NOT REMOVE

THIS PRODUCT LABEL

4233 CLARK RD #20

SARASOTA, FL 34233 • 941-923-3461

LotStickerLotSticker

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
312172oxygen 99 % Gas for InhalationPSN17
312172oxygen 99 % Gas for InhalationSCD17

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53683-0001-1Oxygen180 L in 1 CYLINDERGAS18017
53683-0001-2Oxygen240 L in 1 CYLINDERGAS24017
53683-0001-3Oxygen415 L in 1 CYLINDERGAS41517
53683-0001-4Oxygen682 L in 1 CYLINDERGAS68217
53683-0001-5Oxygen640 L in 1 CYLINDERGAS64017
53683-0001-6Oxygen1738 L in 1 CYLINDERGAS173817
53683-0001-7Oxygen3455 L in 1 CYLINDERGAS345517
53683-0001-8Oxygen7080 L in 1 CYLINDERGAS708017

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OxygenACTIVE INGREDIENTS88TT140651
OxygenACTIVE MOIETYS88TT140651

Products#

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

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

NDC Codes#

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
OXYGENS88TT14065ACTIB

Source Document#

Source XML

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
OxygenOXYGENMedox Corporation5baca5cc-47a4-4a01-bf1f-7ebc5e2253262025-12-30Exact identifier
ndc (package): 53683-0001-4
ndc (package): 53683-0001-6
ndc (package): 53683-0001-1
ndc (package): 53683-0001-3
ndc (package): 53683-0001-8
ndc (package): 53683-0001-7
ndc (package): 53683-0001-5
ndc (package): 53683-0001-2
ndc (product): 53683-0001
ndc11 (package): 53683000107
ndc11 (package): 53683000101
ndc11 (package): 53683000104
ndc11 (package): 53683000105
ndc11 (package): 53683000102
ndc11 (package): 53683000103
ndc11 (package): 53683000106
ndc11 (package): 53683000108
spl id: 47317ad1-0379-c236-e063-6394a90ab118
spl set id: 5baca5cc-47a4-4a01-bf1f-7ebc5e225326

Reported adverse events (FAERS/openFDA)#

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