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
- C&C Oxygen Company
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 8fe7827e-f28b-454c-ac0b-3ece3966f301
- SPL ID
- 3e796c66-c66a-b1a2-e063-6294a90aba69
- Version
- 28
- Effective date
- 2025-10-28
- 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 05:14:46
| 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 | 205865 | derived:openfda.application_number |
| application number | NDA205865 | openfda.application_number | |
| brand name | Oxygen | openfda.brand_name | |
| generic name | OXYGEN | openfda.generic_name | |
| manufacturer name | C&C Oxygen Company | openfda.manufacturer_name | |
| ndc | package | 50322-005-07 | openfda.package_ndc |
| ndc | package | 50322-005-01 | openfda.package_ndc |
| ndc | package | 50322-005-04 | openfda.package_ndc |
| ndc | package | 50322-005-05 | openfda.package_ndc |
| ndc | package | 50322-005-03 | openfda.package_ndc |
| ndc | package | 50322-005-02 | openfda.package_ndc |
| ndc | package | 50322-005-09 | openfda.package_ndc |
| ndc | package | 50322-005-08 | openfda.package_ndc |
| ndc | package | 50322-005-06 | openfda.package_ndc |
| ndc | product | 50322-005 | openfda.product_ndc |
| ndc11 | package | 50322000505 | derived:openfda.package_ndc |
| ndc11 | package | 50322000503 | derived:openfda.package_ndc |
| ndc11 | package | 50322000509 | derived:openfda.package_ndc |
| ndc11 | package | 50322000502 | derived:openfda.package_ndc |
| ndc11 | package | 50322000506 | derived:openfda.package_ndc |
| ndc11 | package | 50322000508 | derived:openfda.package_ndc |
| ndc11 | package | 50322000507 | derived:openfda.package_ndc |
| ndc11 | package | 50322000501 | derived:openfda.package_ndc |
| ndc11 | package | 50322000504 | derived:openfda.package_ndc |
| rxcui | 312172 | openfda.rxcui | |
| spl id | 3e796c66-c66a-b1a2-e063-6294a90aba69 | id | |
| spl set id | 8fe7827e-f28b-454c-ac0b-3ece3966f301 | set_id | |
| unii | S88TT14065 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.