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
- Fitzsimmons Surgical Supply, Inc
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- dc94cdc8-5696-4e17-ae0c-81a3ff2b8751
- SPL ID
- 419cf410-e0f0-5526-e063-6394a90a1b26
- Version
- 19
- Effective date
- 2025-10-20
- Source export date
- 2026-11-06
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/90742968499056f8845d54427ea2950526b02c3f289aedd40679ed8e120a0e89/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
- Import run
- 20261106T075659Z
- Imported at
- 2026-11-06 08:42:21
| 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 | Fitzsimmons Surgical Supply, Inc | openfda.manufacturer_name | |
| ndc | package | 59842-012-04 | openfda.package_ndc |
| ndc | package | 59842-012-05 | openfda.package_ndc |
| ndc | package | 59842-012-14 | openfda.package_ndc |
| ndc | package | 59842-012-09 | openfda.package_ndc |
| ndc | package | 59842-012-07 | openfda.package_ndc |
| ndc | package | 59842-012-13 | openfda.package_ndc |
| ndc | package | 59842-012-06 | openfda.package_ndc |
| ndc | package | 59842-012-10 | openfda.package_ndc |
| ndc | package | 59842-012-08 | openfda.package_ndc |
| ndc | product | 59842-012 | openfda.product_ndc |
| ndc11 | package | 59842001214 | derived:openfda.package_ndc |
| ndc11 | package | 59842001210 | derived:openfda.package_ndc |
| ndc11 | package | 59842001205 | derived:openfda.package_ndc |
| ndc11 | package | 59842001207 | derived:openfda.package_ndc |
| ndc11 | package | 59842001204 | derived:openfda.package_ndc |
| ndc11 | package | 59842001208 | derived:openfda.package_ndc |
| ndc11 | package | 59842001209 | derived:openfda.package_ndc |
| ndc11 | package | 59842001206 | derived:openfda.package_ndc |
| ndc11 | package | 59842001213 | derived:openfda.package_ndc |
| rxcui | 312172 | openfda.rxcui | |
| spl id | 419cf410-e0f0-5526-e063-6394a90a1b26 | id | |
| spl set id | dc94cdc8-5696-4e17-ae0c-81a3ff2b8751 | set_id | |
| unii | S88TT14065 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.