FDA.reportPublic FDA data

Oxygen

Manufacturer
Clinical 1 Home Medical, Inc.
Effective date
2025-10-28
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-05-31 22:03:33

Label at a glance#

ProductOxygen
Active ingredientOXYGEN
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

OXYGEN, COMPRESSED USP

UN 1072

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. Use only with equipment of compatible materials of construction and rated for cylinder pressure. Use only with equipment cleaned for oxygen service. 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.

DO NOT REMOVE THIS PRODUCT LABEL.

WARNING: No smoking or vaping. 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. Produced by Air Liquefaction.

NO SMOKING

NO VAPING

Clinical 1 Home Medical

65 Mathewson Drive Unit E

Weymouth, MA 02189

800-261-5737

CAS NO: 7782-44-7

Contents Size

248 Liters C

415 Liters D

682 Liters E

3455 Liters M

6900 Liters H

Liters Other oxygen 2025oxygen 2025

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
312172oxygen 99 % Gas for InhalationPSN7
312172oxygen 99 % Gas for InhalationSCD7

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
65919-004-01Oxygen170 L in 1 CYLINDERGAS1707
65919-004-02Oxygen248 L in 1 CYLINDERGAS2487
65919-004-03Oxygen415 L in 1 CYLINDERGAS4157
65919-004-04Oxygen682 L in 1 CYLINDERGAS6827
65919-004-05Oxygen3455 L in 1 CYLINDERGAS34557
65919-004-06Oxygen6900 L in 1 CYLINDERGAS69007
65919-004-07Oxygen31 L in 1 DEWARGAS317
65919-004-08Oxygen41 L in 1 DEWARGAS417

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
65919-00465919-004-01, 65919-004-02, 65919-004-03, 65919-004-04, 65919-004-05, 65919-004-06, 65919-004-07, 65919-004-08

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
62024-10-10full-release2026-05-31 21:14:14

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
OxygenOXYGENClinical 1 Home Medical, Inc.9aefc914-6bed-6f56-e053-2995a90a846a2025-10-28Exact identifier
ndc (package): 65919-004-03
ndc (package): 65919-004-08
ndc (package): 65919-004-07
ndc (package): 65919-004-05
ndc (package): 65919-004-02
ndc (package): 65919-004-06
ndc (package): 65919-004-04
ndc (package): 65919-004-01
ndc (product): 65919-004
ndc11 (package): 65919000405
ndc11 (package): 65919000406
ndc11 (package): 65919000402
ndc11 (package): 65919000408
ndc11 (package): 65919000401
ndc11 (package): 65919000407
ndc11 (package): 65919000403
ndc11 (package): 65919000404
spl id: 423bf61d-cc15-4f40-e063-6294a90aae3c
spl set id: 9aefc914-6bed-6f56-e053-2995a90a846a

Reported adverse events (FAERS/openFDA)#

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