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
- Island Equipment Company
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- b2210399-35ec-4c29-a551-4b0e62a60408
- SPL ID
- 49627f0f-f289-d45e-e063-6394a90aa4a9
- Version
- 117
- Effective date
- 2026-01-27
- Source export date
- 2026-10-12
- 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/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:43:23
| 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 | Island Equipment Company | openfda.manufacturer_name | |
| ndc | package | 50153-110-13 | openfda.package_ndc |
| ndc | package | 50153-110-16 | openfda.package_ndc |
| ndc | package | 50153-110-11 | openfda.package_ndc |
| ndc | package | 50153-110-14 | openfda.package_ndc |
| ndc | package | 50153-110-17 | openfda.package_ndc |
| ndc | package | 50153-110-07 | openfda.package_ndc |
| ndc | package | 50153-110-15 | openfda.package_ndc |
| ndc | package | 50153-110-10 | openfda.package_ndc |
| ndc | package | 50153-110-12 | openfda.package_ndc |
| ndc | product | 50153-110 | openfda.product_ndc |
| ndc11 | package | 50153011016 | derived:openfda.package_ndc |
| ndc11 | package | 50153011011 | derived:openfda.package_ndc |
| ndc11 | package | 50153011015 | derived:openfda.package_ndc |
| ndc11 | package | 50153011017 | derived:openfda.package_ndc |
| ndc11 | package | 50153011010 | derived:openfda.package_ndc |
| ndc11 | package | 50153011012 | derived:openfda.package_ndc |
| ndc11 | package | 50153011007 | derived:openfda.package_ndc |
| ndc11 | package | 50153011013 | derived:openfda.package_ndc |
| ndc11 | package | 50153011014 | derived:openfda.package_ndc |
| rxcui | 312172 | openfda.rxcui | |
| spl id | 49627f0f-f289-d45e-e063-6394a90aa4a9 | id | |
| spl set id | b2210399-35ec-4c29-a551-4b0e62a60408 | set_id | |
| unii | S88TT14065 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.