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
- CEE-KAY SUPPLY, INC.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 7a4aa7ab-08a4-4e93-90d7-5329b0e1a61b
- SPL ID
- 4bae463f-cd7b-3ffd-e063-6294a90adb7a
- Version
- 17
- Effective date
- 2026-02-25
- Source export date
- 2026-09-28
- 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/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:35:33
| 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 | CEE-KAY SUPPLY, INC. | openfda.manufacturer_name | |
| ndc | package | 10218-001-07 | openfda.package_ndc |
| ndc | package | 10218-001-02 | openfda.package_ndc |
| ndc | package | 10218-001-04 | openfda.package_ndc |
| ndc | package | 10218-001-05 | openfda.package_ndc |
| ndc | package | 10218-001-01 | openfda.package_ndc |
| ndc | package | 10218-001-03 | openfda.package_ndc |
| ndc | package | 10218-001-06 | openfda.package_ndc |
| ndc | package | 10218-001-08 | openfda.package_ndc |
| ndc | package | 10218-001-09 | openfda.package_ndc |
| ndc | package | 10218-001-10 | openfda.package_ndc |
| ndc | product | 10218-001 | openfda.product_ndc |
| ndc11 | package | 10218000105 | derived:openfda.package_ndc |
| ndc11 | package | 10218000109 | derived:openfda.package_ndc |
| ndc11 | package | 10218000104 | derived:openfda.package_ndc |
| ndc11 | package | 10218000110 | derived:openfda.package_ndc |
| ndc11 | package | 10218000101 | derived:openfda.package_ndc |
| ndc11 | package | 10218000106 | derived:openfda.package_ndc |
| ndc11 | package | 10218000103 | derived:openfda.package_ndc |
| ndc11 | package | 10218000108 | derived:openfda.package_ndc |
| ndc11 | package | 10218000107 | derived:openfda.package_ndc |
| ndc11 | package | 10218000102 | derived:openfda.package_ndc |
| rxcui | 312173 | openfda.rxcui | |
| spl id | 4bae463f-cd7b-3ffd-e063-6294a90adb7a | id | |
| spl set id | 7a4aa7ab-08a4-4e93-90d7-5329b0e1a61b | set_id | |
| unii | S88TT14065 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.