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
- Keen Compressed Gas Co. Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- aefa04b2-fce7-4ec1-bcb6-6cb76c32619b
- SPL ID
- 43d1a690-b44b-1275-e063-6294a90a60e1
- Version
- 14
- Effective date
- 2025-11-17
- Source export date
- 2026-11-06
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/9d5577a314a25811fefbde4767c9b37f3913d9a65fdc458c6336b5aed532339e/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
- Import run
- 20261106T075659Z
- Imported at
- 2026-11-06 08:50:17
| 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 | 205767 | derived:openfda.application_number |
| application number | NDA205767 | openfda.application_number | |
| brand name | OXYGEN | openfda.brand_name | |
| generic name | OXYGEN | openfda.generic_name | |
| manufacturer name | Keen Compressed Gas Co. Inc. | openfda.manufacturer_name | |
| ndc | package | 48273-001-19 | openfda.package_ndc |
| ndc | package | 48273-001-11 | openfda.package_ndc |
| ndc | package | 48273-001-18 | openfda.package_ndc |
| ndc | package | 48273-001-03 | openfda.package_ndc |
| ndc | package | 48273-001-17 | openfda.package_ndc |
| ndc | package | 48273-001-15 | openfda.package_ndc |
| ndc | package | 48273-001-06 | openfda.package_ndc |
| ndc | package | 48273-001-02 | openfda.package_ndc |
| ndc | package | 48273-001-20 | openfda.package_ndc |
| ndc | package | 48273-001-13 | openfda.package_ndc |
| ndc | package | 48273-001-09 | openfda.package_ndc |
| ndc | package | 48273-001-10 | openfda.package_ndc |
| ndc | package | 48273-001-04 | openfda.package_ndc |
| ndc | package | 48273-001-08 | openfda.package_ndc |
| ndc | package | 48273-001-01 | openfda.package_ndc |
| ndc | package | 48273-001-12 | openfda.package_ndc |
| ndc | package | 48273-001-21 | openfda.package_ndc |
| ndc | package | 48273-001-14 | openfda.package_ndc |
| ndc | package | 48273-001-07 | openfda.package_ndc |
| ndc | package | 48273-001-16 | openfda.package_ndc |
| ndc | product | 48273-001 | openfda.product_ndc |
| ndc11 | package | 48273000108 | derived:openfda.package_ndc |
| ndc11 | package | 48273000102 | derived:openfda.package_ndc |
| ndc11 | package | 48273000117 | derived:openfda.package_ndc |
| ndc11 | package | 48273000104 | derived:openfda.package_ndc |
| ndc11 | package | 48273000107 | derived:openfda.package_ndc |
| ndc11 | package | 48273000120 | derived:openfda.package_ndc |
| ndc11 | package | 48273000112 | derived:openfda.package_ndc |
| ndc11 | package | 48273000115 | derived:openfda.package_ndc |
| ndc11 | package | 48273000118 | derived:openfda.package_ndc |
| ndc11 | package | 48273000121 | derived:openfda.package_ndc |
| ndc11 | package | 48273000116 | derived:openfda.package_ndc |
| ndc11 | package | 48273000111 | derived:openfda.package_ndc |
| ndc11 | package | 48273000109 | derived:openfda.package_ndc |
| ndc11 | package | 48273000114 | derived:openfda.package_ndc |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.