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
- 2026-10-27
- 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/2026-10-27/9122bd1bdced046e8f62ea012d80757473b7d83ea1faeea61faef490e06fd630/drug-label-0014-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 21:09:33
| 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.