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
- Bay State Medical, Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- c4252954-1f45-4b02-a8ee-b8d0f195725a
- SPL ID
- 416047a6-26e1-77cc-e063-6394a90ac05e
- Version
- 17
- Effective date
- 2025-10-17
- Source export date
- 2026-10-12
- 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/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:57:04
| 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 | Bay State Medical, Inc. | openfda.manufacturer_name | |
| ndc | package | 62481-4565-4 | openfda.package_ndc |
| ndc | package | 62481-4565-7 | openfda.package_ndc |
| ndc | package | 62481-4565-6 | openfda.package_ndc |
| ndc | product | 62481-4565 | openfda.product_ndc |
| ndc11 | package | 62481456506 | derived:openfda.package_ndc |
| ndc11 | package | 62481456504 | derived:openfda.package_ndc |
| ndc11 | package | 62481456507 | derived:openfda.package_ndc |
| rxcui | 312172 | openfda.rxcui | |
| spl id | 416047a6-26e1-77cc-e063-6394a90ac05e | id | |
| spl set id | c4252954-1f45-4b02-a8ee-b8d0f195725a | set_id | |
| unii | S88TT14065 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.