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
- Central Drug Dorado Corp.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 34a27f1a-c6fa-5a34-e063-6394a90aa2d3
- SPL ID
- 4745853f-39f0-18a9-e063-6394a90a26f5
- Version
- 3
- Effective date
- 2025-12-31
- Source export date
- 2026-10-12
- Source partition
- 10
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:27:35
| 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 | Central Drug Dorado Corp. | openfda.manufacturer_name | |
| ndc | package | 85674-001-04 | openfda.package_ndc |
| ndc | package | 85674-001-03 | openfda.package_ndc |
| ndc | package | 85674-001-10 | openfda.package_ndc |
| ndc | package | 85674-001-01 | openfda.package_ndc |
| ndc | package | 85674-001-07 | openfda.package_ndc |
| ndc | package | 85674-001-05 | openfda.package_ndc |
| ndc | package | 85674-001-09 | openfda.package_ndc |
| ndc | package | 85674-001-11 | openfda.package_ndc |
| ndc | package | 85674-001-06 | openfda.package_ndc |
| ndc | package | 85674-001-02 | openfda.package_ndc |
| ndc | package | 85674-001-12 | openfda.package_ndc |
| ndc | package | 85674-001-08 | openfda.package_ndc |
| ndc | product | 85674-001 | openfda.product_ndc |
| ndc11 | package | 85674000109 | derived:openfda.package_ndc |
| ndc11 | package | 85674000101 | derived:openfda.package_ndc |
| ndc11 | package | 85674000106 | derived:openfda.package_ndc |
| ndc11 | package | 85674000111 | derived:openfda.package_ndc |
| ndc11 | package | 85674000102 | derived:openfda.package_ndc |
| ndc11 | package | 85674000108 | derived:openfda.package_ndc |
| ndc11 | package | 85674000103 | derived:openfda.package_ndc |
| ndc11 | package | 85674000107 | derived:openfda.package_ndc |
| ndc11 | package | 85674000104 | derived:openfda.package_ndc |
| ndc11 | package | 85674000112 | derived:openfda.package_ndc |
| ndc11 | package | 85674000110 | derived:openfda.package_ndc |
| ndc11 | package | 85674000105 | derived:openfda.package_ndc |
| rxcui | 312172 | openfda.rxcui | |
| spl id | 4745853f-39f0-18a9-e063-6394a90a26f5 | id | |
| spl set id | 34a27f1a-c6fa-5a34-e063-6394a90aa2d3 | set_id | |
| unii | S88TT14065 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.