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
- BUCKEYE WELDING SUPPLY COMPANY, INC.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- e1fab9b0-3c7b-8625-e053-2a95a90a5a76
- SPL ID
- 44fb9799-1c75-b042-e063-6394a90a9aec
- Version
- 3
- Effective date
- 2025-12-02
- Source export date
- 2026-09-28
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:54:43
| 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 | 205827 | derived:openfda.application_number |
| application number | NDA205827 | openfda.application_number | |
| brand name | Oxygen | openfda.brand_name | |
| generic name | OXYGEN | openfda.generic_name | |
| manufacturer name | BUCKEYE WELDING SUPPLY COMPANY, INC. | openfda.manufacturer_name | |
| ndc | package | 53729-0002-8 | openfda.package_ndc |
| ndc | package | 53729-0002-6 | openfda.package_ndc |
| ndc | package | 53729-0002-5 | openfda.package_ndc |
| ndc | package | 53729-0002-1 | openfda.package_ndc |
| ndc | package | 53729-0002-7 | openfda.package_ndc |
| ndc | package | 53729-0002-3 | openfda.package_ndc |
| ndc | package | 53729-0002-4 | openfda.package_ndc |
| ndc | package | 53729-0002-2 | openfda.package_ndc |
| ndc | product | 53729-0002 | openfda.product_ndc |
| ndc11 | package | 53729000202 | derived:openfda.package_ndc |
| ndc11 | package | 53729000201 | derived:openfda.package_ndc |
| ndc11 | package | 53729000208 | derived:openfda.package_ndc |
| ndc11 | package | 53729000204 | derived:openfda.package_ndc |
| ndc11 | package | 53729000205 | derived:openfda.package_ndc |
| ndc11 | package | 53729000203 | derived:openfda.package_ndc |
| ndc11 | package | 53729000206 | derived:openfda.package_ndc |
| ndc11 | package | 53729000207 | derived:openfda.package_ndc |
| rxcui | 348831 | openfda.rxcui | |
| spl id | 44fb9799-1c75-b042-e063-6394a90a9aec | id | |
| spl set id | e1fab9b0-3c7b-8625-e053-2a95a90a5a76 | set_id | |
| unii | S88TT14065 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.