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
- Island Supply Welding Co Inc
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 9a84e50c-504a-4e7d-8595-ebce7d78d127
- SPL ID
- 44227a2b-c111-4713-e063-6394a90aaca2
- Version
- 15
- Effective date
- 2025-11-21
- Source export date
- 2026-09-28
- Source partition
- 4
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:25:26
| 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 | 205889 | derived:openfda.application_number |
| application number | NDA205889 | openfda.application_number | |
| brand name | Oxygen | openfda.brand_name | |
| generic name | OXYGEN | openfda.generic_name | |
| manufacturer name | Island Supply Welding Co Inc | openfda.manufacturer_name | |
| ndc | package | 21624-001-26 | openfda.package_ndc |
| ndc | package | 21624-001-18 | openfda.package_ndc |
| ndc | package | 21624-001-22 | openfda.package_ndc |
| ndc | package | 21624-001-38 | openfda.package_ndc |
| ndc | package | 21624-001-23 | openfda.package_ndc |
| ndc | package | 21624-001-36 | openfda.package_ndc |
| ndc | package | 21624-001-30 | openfda.package_ndc |
| ndc | package | 21624-001-34 | openfda.package_ndc |
| ndc | package | 21624-001-28 | openfda.package_ndc |
| ndc | package | 21624-001-32 | openfda.package_ndc |
| ndc | package | 21624-001-33 | openfda.package_ndc |
| ndc | package | 21624-001-25 | openfda.package_ndc |
| ndc | package | 21624-001-39 | openfda.package_ndc |
| ndc | package | 21624-001-12 | openfda.package_ndc |
| ndc | package | 21624-001-20 | openfda.package_ndc |
| ndc | package | 21624-001-31 | openfda.package_ndc |
| ndc | package | 21624-001-15 | openfda.package_ndc |
| ndc | package | 21624-001-24 | openfda.package_ndc |
| ndc | package | 21624-001-35 | openfda.package_ndc |
| ndc | package | 21624-001-11 | openfda.package_ndc |
| ndc | package | 21624-001-27 | openfda.package_ndc |
| ndc | package | 21624-001-37 | openfda.package_ndc |
| ndc | package | 21624-001-40 | openfda.package_ndc |
| ndc | package | 21624-001-29 | openfda.package_ndc |
| ndc | package | 21624-001-13 | openfda.package_ndc |
| ndc | package | 21624-001-16 | openfda.package_ndc |
| ndc | package | 21624-001-21 | openfda.package_ndc |
| ndc | package | 21624-001-19 | openfda.package_ndc |
| ndc | package | 21624-001-17 | openfda.package_ndc |
| ndc | package | 21624-001-14 | openfda.package_ndc |
| ndc | product | 21624-001 | openfda.product_ndc |
| ndc11 | package | 21624000129 | derived:openfda.package_ndc |
| ndc11 | package | 21624000117 | derived:openfda.package_ndc |
| ndc11 | package | 21624000137 | derived:openfda.package_ndc |
| ndc11 | package | 21624000132 | derived:openfda.package_ndc |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.