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
- Minneapolis Oxygen Company
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 71e087d2-b148-444d-b2d7-09a4cd3d228f
- SPL ID
- 44eb7405-d089-15eb-e063-6394a90a7917
- Version
- 17
- Effective date
- 2025-12-01
- Source export date
- 2026-10-30
- Source partition
- 13
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-30/8d15bdc5962e7531569eaeb5b1b2e4919574d40a6782ab67345a27b890175a00/drug-label-0013-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 19:58:44
| 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 |
|---|---|---|---|
| application applno | NDA | 205767 | derived:openfda.application_number |
| application number | NDA205767 | openfda.application_number | |
| brand name | Oxygen | openfda.brand_name | |
| generic name | OXYGEN | openfda.generic_name | |
| manufacturer name | Minneapolis Oxygen Company | openfda.manufacturer_name | |
| ndc | package | 55147-001-14 | openfda.package_ndc |
| ndc | package | 55147-001-13 | openfda.package_ndc |
| ndc | package | 55147-001-07 | openfda.package_ndc |
| ndc | package | 55147-001-00 | openfda.package_ndc |
| ndc | package | 55147-001-16 | openfda.package_ndc |
| ndc | package | 55147-001-12 | openfda.package_ndc |
| ndc | package | 55147-001-06 | openfda.package_ndc |
| ndc | package | 55147-001-11 | openfda.package_ndc |
| ndc | package | 55147-001-17 | openfda.package_ndc |
| ndc | package | 55147-001-05 | openfda.package_ndc |
| ndc | package | 55147-001-10 | openfda.package_ndc |
| ndc | package | 55147-001-08 | openfda.package_ndc |
| ndc | package | 55147-001-09 | openfda.package_ndc |
| ndc | package | 55147-001-02 | openfda.package_ndc |
| ndc | package | 55147-001-01 | openfda.package_ndc |
| ndc | package | 55147-001-03 | openfda.package_ndc |
| ndc | package | 55147-001-04 | openfda.package_ndc |
| ndc | product | 55147-001 | openfda.product_ndc |
| ndc11 | package | 55147000102 | derived:openfda.package_ndc |
| ndc11 | package | 55147000110 | derived:openfda.package_ndc |
| ndc11 | package | 55147000100 | derived:openfda.package_ndc |
| ndc11 | package | 55147000106 | derived:openfda.package_ndc |
| ndc11 | package | 55147000105 | derived:openfda.package_ndc |
| ndc11 | package | 55147000112 | derived:openfda.package_ndc |
| ndc11 | package | 55147000104 | derived:openfda.package_ndc |
| ndc11 | package | 55147000109 | derived:openfda.package_ndc |
| ndc11 | package | 55147000111 | derived:openfda.package_ndc |
| ndc11 | package | 55147000114 | derived:openfda.package_ndc |
| ndc11 | package | 55147000113 | derived:openfda.package_ndc |
| ndc11 | package | 55147000107 | derived:openfda.package_ndc |
| ndc11 | package | 55147000103 | derived:openfda.package_ndc |
| ndc11 | package | 55147000117 | derived:openfda.package_ndc |
| ndc11 | package | 55147000108 | derived:openfda.package_ndc |
| ndc11 | package | 55147000116 | derived:openfda.package_ndc |
| ndc11 | package | 55147000101 | derived:openfda.package_ndc |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.