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 Health Services
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 84626ce5-9a3c-3e6c-e053-2991aa0aa449
- SPL ID
- 45b06d81-4e14-aae2-e063-6394a90a32c5
- Version
- 9
- Effective date
- 2025-12-11
- Source export date
- 2026-09-28
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:16:58
| 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 Health Services | openfda.manufacturer_name | |
| ndc | package | 67480-001-02 | openfda.package_ndc |
| ndc | package | 67480-001-01 | openfda.package_ndc |
| ndc | package | 67480-001-03 | openfda.package_ndc |
| ndc | product | 67480-001 | openfda.product_ndc |
| ndc11 | package | 67480000101 | derived:openfda.package_ndc |
| ndc11 | package | 67480000102 | derived:openfda.package_ndc |
| ndc11 | package | 67480000103 | derived:openfda.package_ndc |
| rxcui | 312172 | openfda.rxcui | |
| spl id | 45b06d81-4e14-aae2-e063-6394a90a32c5 | id | |
| spl set id | 84626ce5-9a3c-3e6c-e053-2991aa0aa449 | set_id | |
| unii | S88TT14065 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.