Oxygen
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Oxygen
- Generic name
- OXYGEN
- Manufacturer
- Frances Mahon Deaconess Hospital Home Oxygen
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 93ca8d91-861c-4a6f-b324-02f6b9019e37
- SPL ID
- 41b06fe5-a070-06a6-e063-6394a90a5f2e
- Version
- 16
- Effective date
- 2025-10-21
- Source export date
- 2026-09-28
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:18:42
| Harmonized routes |
|---|
| RESPIRATORY (INHALATION) |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| brand name | Oxygen | openfda.brand_name | |
| generic name | OXYGEN | openfda.generic_name | |
| manufacturer name | Frances Mahon Deaconess Hospital Home Oxygen | openfda.manufacturer_name | |
| ndc | package | 65217-0001-1 | openfda.package_ndc |
| ndc | package | 65217-0001-2 | openfda.package_ndc |
| ndc | package | 65217-0001-3 | openfda.package_ndc |
| ndc | product | 65217-0001 | openfda.product_ndc |
| ndc11 | package | 65217000103 | derived:openfda.package_ndc |
| ndc11 | package | 65217000101 | derived:openfda.package_ndc |
| ndc11 | package | 65217000102 | derived:openfda.package_ndc |
| rxcui | 312172 | openfda.rxcui | |
| spl id | 41b06fe5-a070-06a6-e063-6394a90a5f2e | id | |
| spl set id | 93ca8d91-861c-4a6f-b324-02f6b9019e37 | set_id | |
| unii | S88TT14065 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.