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
- All-Weld Products Corp dba All-Weld Products Group
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 7cd44342-88e5-fe89-e053-2a91aa0a13a3
- SPL ID
- 4149aadf-3dcb-a44a-e063-6394a90a27f9
- Version
- 7
- Effective date
- 2025-10-16
- Source export date
- 2026-11-06
- 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/2026-11-06/9d5577a314a25811fefbde4767c9b37f3913d9a65fdc458c6336b5aed532339e/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
- Import run
- 20261106T075659Z
- Imported at
- 2026-11-06 08:50:20
| 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 | All-Weld Products Corp dba All-Weld Products Group | openfda.manufacturer_name | |
| ndc | package | 50517-123-01 | openfda.package_ndc |
| ndc | package | 50517-123-07 | openfda.package_ndc |
| ndc | package | 50517-123-06 | openfda.package_ndc |
| ndc | package | 50517-123-04 | openfda.package_ndc |
| ndc | package | 50517-123-03 | openfda.package_ndc |
| ndc | package | 50517-123-08 | openfda.package_ndc |
| ndc | package | 50517-123-05 | openfda.package_ndc |
| ndc | package | 50517-123-02 | openfda.package_ndc |
| ndc | product | 50517-123 | openfda.product_ndc |
| ndc11 | package | 50517012308 | derived:openfda.package_ndc |
| ndc11 | package | 50517012305 | derived:openfda.package_ndc |
| ndc11 | package | 50517012303 | derived:openfda.package_ndc |
| ndc11 | package | 50517012302 | derived:openfda.package_ndc |
| ndc11 | package | 50517012307 | derived:openfda.package_ndc |
| ndc11 | package | 50517012306 | derived:openfda.package_ndc |
| ndc11 | package | 50517012301 | derived:openfda.package_ndc |
| ndc11 | package | 50517012304 | derived:openfda.package_ndc |
| rxcui | 312172 | openfda.rxcui | |
| spl id | 4149aadf-3dcb-a44a-e063-6394a90a27f9 | id | |
| spl set id | 7cd44342-88e5-fe89-e053-2a91aa0a13a3 | set_id | |
| unii | S88TT14065 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.