FDA.reportPublic FDA data

Oxygen

Manufacturer
HARTMAN BROTHERS, INC.
Effective date
2025-10-24
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
14
Source
full-release
Hydrated at
2026-05-31 22:03:04

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. 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 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 with 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.

CAS 7782-44-7 DO NOT REMOVE THIS PRODUCT LABEL.

NO SMOKING

NO VAPING

HARTMAN BROTHERS INC.

821 21 ½ Road Grand Junction, CO 81505 970-240-8535 oxygen 2025oxygen 2025

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
312172oxygen 99 % Gas for InhalationPSN14
312172oxygen 99 % Gas for InhalationSCD14

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49204-001-01Oxygen420 L in 1 CYLINDERGAS42014
49204-001-02Oxygen690 L in 1 CYLINDERGAS69014
49204-001-03Oxygen3160 L in 1 CYLINDERGAS316014
49204-001-04Oxygen3470 L in 1 CYLINDERGAS347014
49204-001-05Oxygen5270 L in 1 CYLINDERGAS527014
49204-001-06Oxygen6270 L in 1 CYLINDERGAS627014
49204-001-07Oxygen6900 L in 1 CYLINDERGAS690014
49204-001-08Oxygen7060 L in 1 CYLINDERGAS706014
49204-001-09Oxygen7760 L in 1 CYLINDERGAS776014
49204-001-10Oxygen8510 L in 1 CYLINDERGAS851014
49204-001-11Oxygen9340 L in 1 CYLINDERGAS934014
49204-001-12Oxygen42 L in 1 CYLINDERGAS4214
49204-001-13Oxygen113 L in 1 CYLINDERGAS11314
49204-001-14Oxygen164 L in 1 CYLINDERGAS16414
49204-001-15Oxygen139 L in 1 CYLINDERGAS13914
49204-001-16Oxygen248 L in 1 CYLINDERGAS24814
49204-001-17Oxygen647 L in 1 CYLINDERGAS64714
49204-001-18Oxygen1724 L in 1 CYLINDERGAS172414
49204-001-19Oxygen1147 L in 1 CYLINDERGAS114714
49204-001-20Oxygen153903 L in 1 CYLINDERGAS15390314

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#

Product NDC, Package NDC table
Product NDCPackage NDC
49204-00149204-001-01, 49204-001-02, 49204-001-03, 49204-001-04, 49204-001-05, 49204-001-06, 49204-001-07, 49204-001-08, 49204-001-09, 49204-001-10, 49204-001-11, 49204-001-12, 49204-001-13, 49204-001-14, 49204-001-15, 49204-001-16, 49204-001-17, 49204-001-18, 49204-001-19, 49204-001-20

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

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
132025-02-17full-release2026-05-31 21:26:11

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
OxygenOXYGENHARTMAN BROTHERS, INC.b8a4f8fa-2c11-4ee4-850d-d1ee80fb00002025-10-24Exact identifier
ndc (package): 49204-001-19
ndc (package): 49204-001-20
ndc (package): 49204-001-13
ndc (package): 49204-001-09
ndc (package): 49204-001-05
ndc (package): 49204-001-15
ndc (package): 49204-001-06
ndc (package): 49204-001-08
ndc (package): 49204-001-17
ndc (package): 49204-001-14
ndc (package): 49204-001-16
ndc (package): 49204-001-10
ndc (package): 49204-001-11
ndc (package): 49204-001-01
ndc (package): 49204-001-18
ndc (package): 49204-001-03
ndc (package): 49204-001-07
ndc (package): 49204-001-02
ndc (package): 49204-001-04
ndc (package): 49204-001-12
ndc (product): 49204-001
ndc11 (package): 49204000117
ndc11 (package): 49204000101
ndc11 (package): 49204000118
ndc11 (package): 49204000113
ndc11 (package): 49204000112
ndc11 (package): 49204000104
ndc11 (package): 49204000114
ndc11 (package): 49204000109
ndc11 (package): 49204000116
ndc11 (package): 49204000115
ndc11 (package): 49204000105
ndc11 (package): 49204000103
ndc11 (package): 49204000110
ndc11 (package): 49204000119
ndc11 (package): 49204000120
ndc11 (package): 49204000107
ndc11 (package): 49204000102
ndc11 (package): 49204000106
ndc11 (package): 49204000108
ndc11 (package): 49204000111
spl id: 41edeb0c-4d63-d4fb-e063-6294a90aec6c
spl set id: b8a4f8fa-2c11-4ee4-850d-d1ee80fb0000

Reported adverse events (FAERS/openFDA)#

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