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
- Thumb Welding Supplies Inc
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- e22127b4-c9d9-458e-b196-4b000b89d781
- SPL ID
- c17d6d32-fa30-4b73-9fae-bd019efa2c27
- Version
- 8
- Effective date
- 2024-10-28
- Source export date
- 2026-09-28
- Source partition
- 10
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:09:23
| 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 |
|---|---|---|---|
| application applno | NDA | 205840 | derived:openfda.application_number |
| application number | NDA205840 | openfda.application_number | |
| brand name | OXYGEN | openfda.brand_name | |
| generic name | OXYGEN | openfda.generic_name | |
| manufacturer name | Thumb Welding Supplies Inc | openfda.manufacturer_name | |
| ndc | package | 55127-001-03 | openfda.package_ndc |
| ndc | package | 55127-001-01 | openfda.package_ndc |
| ndc | package | 55127-001-07 | openfda.package_ndc |
| ndc | package | 55127-001-04 | openfda.package_ndc |
| ndc | package | 55127-001-06 | openfda.package_ndc |
| ndc | package | 55127-001-08 | openfda.package_ndc |
| ndc | package | 55127-001-02 | openfda.package_ndc |
| ndc | package | 55127-001-05 | openfda.package_ndc |
| ndc | product | 55127-001 | openfda.product_ndc |
| ndc11 | package | 55127000103 | derived:openfda.package_ndc |
| ndc11 | package | 55127000101 | derived:openfda.package_ndc |
| ndc11 | package | 55127000105 | derived:openfda.package_ndc |
| ndc11 | package | 55127000108 | derived:openfda.package_ndc |
| ndc11 | package | 55127000107 | derived:openfda.package_ndc |
| ndc11 | package | 55127000102 | derived:openfda.package_ndc |
| ndc11 | package | 55127000106 | derived:openfda.package_ndc |
| ndc11 | package | 55127000104 | derived:openfda.package_ndc |
| rxcui | 312172 | openfda.rxcui | |
| spl id | c17d6d32-fa30-4b73-9fae-bd019efa2c27 | id | |
| spl set id | e22127b4-c9d9-458e-b196-4b000b89d781 | set_id | |
| unii | S88TT14065 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.