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
- Abilene Oxygen Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 55c8ac5c-c57a-438b-886f-42d4817a7208
- SPL ID
- 463d4b55-9ba4-76fc-e063-6294a90abc04
- Version
- 9
- Effective date
- 2025-12-18
- Source export date
- 2026-10-30
- Source partition
- 6
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-30/e37bebe0ee356110e46fe9b102632217cd5fd64caa93a64cf6ef0d92a0bfdb4c/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 18:50:13
| 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 | Abilene Oxygen Inc. | openfda.manufacturer_name | |
| ndc | package | 50809-001-18 | openfda.package_ndc |
| ndc | package | 50809-001-15 | openfda.package_ndc |
| ndc | package | 50809-001-14 | openfda.package_ndc |
| ndc | package | 50809-001-19 | openfda.package_ndc |
| ndc | package | 50809-001-17 | openfda.package_ndc |
| ndc | package | 50809-001-10 | openfda.package_ndc |
| ndc | package | 50809-001-11 | openfda.package_ndc |
| ndc | package | 50809-001-13 | openfda.package_ndc |
| ndc | package | 50809-001-12 | openfda.package_ndc |
| ndc | package | 50809-001-02 | openfda.package_ndc |
| ndc | package | 50809-001-09 | openfda.package_ndc |
| ndc | package | 50809-001-16 | openfda.package_ndc |
| ndc | product | 50809-001 | openfda.product_ndc |
| ndc11 | package | 50809000111 | derived:openfda.package_ndc |
| ndc11 | package | 50809000117 | derived:openfda.package_ndc |
| ndc11 | package | 50809000113 | derived:openfda.package_ndc |
| ndc11 | package | 50809000109 | derived:openfda.package_ndc |
| ndc11 | package | 50809000119 | derived:openfda.package_ndc |
| ndc11 | package | 50809000110 | derived:openfda.package_ndc |
| ndc11 | package | 50809000118 | derived:openfda.package_ndc |
| ndc11 | package | 50809000115 | derived:openfda.package_ndc |
| ndc11 | package | 50809000112 | derived:openfda.package_ndc |
| ndc11 | package | 50809000102 | derived:openfda.package_ndc |
| ndc11 | package | 50809000116 | derived:openfda.package_ndc |
| ndc11 | package | 50809000114 | derived:openfda.package_ndc |
| rxcui | 312172 | openfda.rxcui | |
| spl id | 463d4b55-9ba4-76fc-e063-6294a90abc04 | id | |
| spl set id | 55c8ac5c-c57a-438b-886f-42d4817a7208 | set_id | |
| unii | S88TT14065 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.