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
- Respiratory Home Care and Convalescent Supply Inc
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 7df36cb1-a4d7-07d6-e053-2991aa0aab79
- SPL ID
- 55f34c2d-bf42-c41c-e063-6394a90a07c3
- Version
- 10
- Effective date
- 2026-07-06
- Source export date
- 2026-09-28
- Source partition
- 14
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/db99fd80353afecef4949b48edcaa018be72b966b2360184251eb14df43743f9/drug-label-0014-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:40:10
| 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 | Respiratory Home Care and Convalescent Supply Inc | openfda.manufacturer_name | |
| ndc | package | 58049-123-01 | openfda.package_ndc |
| ndc | package | 58049-123-02 | openfda.package_ndc |
| ndc | package | 58049-123-03 | openfda.package_ndc |
| ndc | product | 58049-123 | openfda.product_ndc |
| ndc11 | package | 58049012303 | derived:openfda.package_ndc |
| ndc11 | package | 58049012301 | derived:openfda.package_ndc |
| ndc11 | package | 58049012302 | derived:openfda.package_ndc |
| rxcui | 312172 | openfda.rxcui | |
| spl id | 55f34c2d-bf42-c41c-e063-6394a90a07c3 | id | |
| spl set id | 7df36cb1-a4d7-07d6-e053-2991aa0aab79 | set_id | |
| unii | S88TT14065 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.