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
- Airtec Gases, LLC
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- b987aa29-71ce-4062-be6c-9400a42751fa
- SPL ID
- 41105f3f-b4d6-a1c1-e063-6394a90aa825
- Version
- 13
- Effective date
- 2025-10-13
- Source export date
- 2026-09-28
- Source partition
- 5
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:34:15
| 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 | 205712 | derived:openfda.application_number |
| application number | NDA205712 | openfda.application_number | |
| brand name | OXYGEN | openfda.brand_name | |
| generic name | OXYGEN | openfda.generic_name | |
| manufacturer name | Airtec Gases, LLC | openfda.manufacturer_name | |
| ndc | package | 24312-001-04 | openfda.package_ndc |
| ndc | package | 24312-001-02 | openfda.package_ndc |
| ndc | package | 24312-001-08 | openfda.package_ndc |
| ndc | package | 24312-001-06 | openfda.package_ndc |
| ndc | package | 24312-001-07 | openfda.package_ndc |
| ndc | package | 24312-001-25 | openfda.package_ndc |
| ndc | package | 24312-001-09 | openfda.package_ndc |
| ndc | package | 24312-001-03 | openfda.package_ndc |
| ndc | package | 24312-001-01 | openfda.package_ndc |
| ndc | package | 24312-001-13 | openfda.package_ndc |
| ndc | package | 24312-001-22 | openfda.package_ndc |
| ndc | package | 24312-001-19 | openfda.package_ndc |
| ndc | package | 24312-001-20 | openfda.package_ndc |
| ndc | package | 24312-001-05 | openfda.package_ndc |
| ndc | package | 24312-001-10 | openfda.package_ndc |
| ndc | package | 24312-001-17 | openfda.package_ndc |
| ndc | package | 24312-001-16 | openfda.package_ndc |
| ndc | package | 24312-001-12 | openfda.package_ndc |
| ndc | package | 24312-001-21 | openfda.package_ndc |
| ndc | package | 24312-001-24 | openfda.package_ndc |
| ndc | package | 24312-001-23 | openfda.package_ndc |
| ndc | package | 24312-001-18 | openfda.package_ndc |
| ndc | package | 24312-001-11 | openfda.package_ndc |
| ndc | package | 24312-001-15 | openfda.package_ndc |
| ndc | package | 24312-001-14 | openfda.package_ndc |
| ndc | product | 24312-001 | openfda.product_ndc |
| ndc11 | package | 24312000117 | derived:openfda.package_ndc |
| ndc11 | package | 24312000123 | derived:openfda.package_ndc |
| ndc11 | package | 24312000118 | derived:openfda.package_ndc |
| ndc11 | package | 24312000106 | derived:openfda.package_ndc |
| ndc11 | package | 24312000105 | derived:openfda.package_ndc |
| ndc11 | package | 24312000122 | derived:openfda.package_ndc |
| ndc11 | package | 24312000108 | derived:openfda.package_ndc |
| ndc11 | package | 24312000119 | derived:openfda.package_ndc |
| ndc11 | package | 24312000111 | derived:openfda.package_ndc |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.