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
- Crumpton Welding Supply & Equipment, Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 8c6b984d-2ace-4534-b441-c2db959a1da1
- SPL ID
- 89ab3145-e256-4d92-8929-767eb49fcde7
- Version
- 12
- Effective date
- 2025-02-10
- Source export date
- 2026-09-28
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:18:19
| 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 | 205889 | derived:openfda.application_number |
| application number | NDA205889 | openfda.application_number | |
| brand name | OXYGEN | openfda.brand_name | |
| generic name | OXYGEN | openfda.generic_name | |
| manufacturer name | Crumpton Welding Supply & Equipment, Inc. | openfda.manufacturer_name | |
| ndc | package | 52568-001-04 | openfda.package_ndc |
| ndc | package | 52568-001-02 | openfda.package_ndc |
| ndc | package | 52568-001-08 | openfda.package_ndc |
| ndc | package | 52568-001-07 | openfda.package_ndc |
| ndc | package | 52568-001-05 | openfda.package_ndc |
| ndc | package | 52568-001-06 | openfda.package_ndc |
| ndc | package | 52568-001-03 | openfda.package_ndc |
| ndc | package | 52568-001-09 | openfda.package_ndc |
| ndc | package | 52568-001-01 | openfda.package_ndc |
| ndc | product | 52568-001 | openfda.product_ndc |
| ndc11 | package | 52568000101 | derived:openfda.package_ndc |
| ndc11 | package | 52568000103 | derived:openfda.package_ndc |
| ndc11 | package | 52568000106 | derived:openfda.package_ndc |
| ndc11 | package | 52568000105 | derived:openfda.package_ndc |
| ndc11 | package | 52568000107 | derived:openfda.package_ndc |
| ndc11 | package | 52568000102 | derived:openfda.package_ndc |
| ndc11 | package | 52568000104 | derived:openfda.package_ndc |
| ndc11 | package | 52568000109 | derived:openfda.package_ndc |
| ndc11 | package | 52568000108 | derived:openfda.package_ndc |
| rxcui | 312172 | openfda.rxcui | |
| spl id | 89ab3145-e256-4d92-8929-767eb49fcde7 | id | |
| spl set id | 8c6b984d-2ace-4534-b441-c2db959a1da1 | set_id | |
| unii | S88TT14065 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.