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
- Eureka Oxygen Company
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 0b776546-e469-41cd-b9d6-d9f6b9e69890
- SPL ID
- 40950add-d52f-50fc-e063-6394a90a2423
- Version
- 12
- Effective date
- 2025-10-07
- Source export date
- 2026-09-28
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:14:45
| 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 | 205712 | derived:openfda.application_number |
| application number | NDA205712 | openfda.application_number | |
| brand name | Oxygen | openfda.brand_name | |
| generic name | OXYGEN | openfda.generic_name | |
| manufacturer name | Eureka Oxygen Company | openfda.manufacturer_name | |
| ndc | package | 66754-001-07 | openfda.package_ndc |
| ndc | package | 66754-001-05 | openfda.package_ndc |
| ndc | package | 66754-001-01 | openfda.package_ndc |
| ndc | package | 66754-001-03 | openfda.package_ndc |
| ndc | package | 66754-001-02 | openfda.package_ndc |
| ndc | package | 66754-001-04 | openfda.package_ndc |
| ndc | package | 66754-001-06 | openfda.package_ndc |
| ndc | product | 66754-001 | openfda.product_ndc |
| ndc11 | package | 66754000104 | derived:openfda.package_ndc |
| ndc11 | package | 66754000101 | derived:openfda.package_ndc |
| ndc11 | package | 66754000103 | derived:openfda.package_ndc |
| ndc11 | package | 66754000106 | derived:openfda.package_ndc |
| ndc11 | package | 66754000102 | derived:openfda.package_ndc |
| ndc11 | package | 66754000107 | derived:openfda.package_ndc |
| ndc11 | package | 66754000105 | derived:openfda.package_ndc |
| rxcui | 312172 | openfda.rxcui | |
| spl id | 40950add-d52f-50fc-e063-6394a90a2423 | id | |
| spl set id | 0b776546-e469-41cd-b9d6-d9f6b9e69890 | set_id | |
| unii | S88TT14065 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.