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
- Huber Supply Co. Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 2d9a54b2-842e-4e8c-8b90-d585418bb5c3
- SPL ID
- b5a73065-51cd-48dc-b401-dccac690eda5
- Version
- 8
- Effective date
- 2024-10-21
- Source export date
- 2026-09-28
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:19:34
| 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 | 205849 | derived:openfda.application_number |
| application number | NDA205849 | openfda.application_number | |
| brand name | Oxygen | openfda.brand_name | |
| generic name | OXYGEN | openfda.generic_name | |
| manufacturer name | Huber Supply Co. Inc. | openfda.manufacturer_name | |
| ndc | package | 60184-001-06 | openfda.package_ndc |
| ndc | package | 60184-001-08 | openfda.package_ndc |
| ndc | package | 60184-001-07 | openfda.package_ndc |
| ndc | package | 60184-001-01 | openfda.package_ndc |
| ndc | package | 60184-001-05 | openfda.package_ndc |
| ndc | package | 60184-001-03 | openfda.package_ndc |
| ndc | package | 60184-001-04 | openfda.package_ndc |
| ndc | package | 60184-001-02 | openfda.package_ndc |
| ndc | package | 60184-001-09 | openfda.package_ndc |
| ndc | product | 60184-001 | openfda.product_ndc |
| ndc11 | package | 60184000104 | derived:openfda.package_ndc |
| ndc11 | package | 60184000103 | derived:openfda.package_ndc |
| ndc11 | package | 60184000101 | derived:openfda.package_ndc |
| ndc11 | package | 60184000108 | derived:openfda.package_ndc |
| ndc11 | package | 60184000107 | derived:openfda.package_ndc |
| ndc11 | package | 60184000106 | derived:openfda.package_ndc |
| ndc11 | package | 60184000105 | derived:openfda.package_ndc |
| ndc11 | package | 60184000102 | derived:openfda.package_ndc |
| ndc11 | package | 60184000109 | derived:openfda.package_ndc |
| rxcui | 312172 | openfda.rxcui | |
| spl id | b5a73065-51cd-48dc-b401-dccac690eda5 | id | |
| spl set id | 2d9a54b2-842e-4e8c-8b90-d585418bb5c3 | set_id | |
| unii | S88TT14065 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.