FDA.reportPublic FDA data

oxygen

Manufacturer
Shaw Oxygen Company Inc
Effective date
2025-12-02
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
16
Source
full-release
Hydrated at
2026-05-31 21:48:03

Label at a glance#

Productoxygen
Active ingredientOXYGEN
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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 required. 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.

DANGER: MAY CAUSE OR INTENSIFY FIRE; OXIDIZER. CONTAINS GAS UNDER PRESSURE; MAY EXPLODE IF HEATED. Obtain, read and follow all safety instructions before use. Keep away from clothing and other combustible materials. Keep valves and fittings free from grease and oil. Use and store only outdoors or with adequate ventilation. Store 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. Use only equipment of compatible materials of construction and rated for cylinder pressure. Use only with equipment cleaned for oxygen service. Do not open valve until connected to equipment prepared for use. Open valve slowly. Close valve after each use and when empty. Protect from sunlight when ambient temperature exceeds 52 C (125 F). Read and follow the Safety Data Sheet (SDS) before use. CAS: 7782-44-7 DO NOT REMOVE THIS PRODUCT LABEL.

Shaw Oxygen Co., Inc.

2914 Desiard St. Monroe, LA 71201

318-387-4115

NO SMOKING

NO VAPING

CONTENTS: LTRS: CU.FT. oxygen 2025oxygen 2025

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
312173oxygen 99.5 % Gas for InhalationPSN16
312173oxygen 99.5 % Gas for InhalationSCD16

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54767-001-09oxygen424 L in 1 CYLINDERGAS42416
54767-001-14oxygen283 L in 1 CYLINDERGAS28316
54767-001-31oxygen3538 L in 1 CYLINDERGAS353816
54767-001-37oxygen7107 L in 1 CYLINDERGAS710716
54767-001-40oxygen8693 L in 1 CYLINDERGAS869316
54767-001-74oxygen39573 L in 1 DEWARGAS3957316
54767-001-80oxygen141868 L in 1 DEWARGAS14186816

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
oxygenACTIVE INGREDIENTS88TT140655
oxygenACTIVE MOIETYS88TT140655

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
54767-00154767-001-14, 54767-001-09, 54767-001-31, 54767-001-37, 54767-001-40, 54767-001-74, 54767-001-80

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

Orange Book application contexts#

All distinct exact application/product contexts derived from this label’s complete NDC list are paginated below.

Orange Book application contexts page 1 of 1 · 1 matching rows.

Source provenance: Browse the complete Orange Book source catalog.

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
oxygenOXYGENShaw Oxygen Company Inc287f2a22-daea-4d64-80a7-2f825852c6a72025-12-02Exact identifier
ndc (package): 54767-001-14
ndc (package): 54767-001-80
ndc (package): 54767-001-40
ndc (package): 54767-001-31
ndc (package): 54767-001-09
ndc (package): 54767-001-37
ndc (package): 54767-001-74
ndc (product): 54767-001
ndc11 (package): 54767000174
ndc11 (package): 54767000114
ndc11 (package): 54767000180
ndc11 (package): 54767000109
ndc11 (package): 54767000140
ndc11 (package): 54767000137
ndc11 (package): 54767000131
spl id: 4500baaa-0a61-0f95-e063-6294a90a1bc5
spl set id: 287f2a22-daea-4d64-80a7-2f825852c6a7

Reported adverse events (FAERS/openFDA)#

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