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
- SYOXSA, Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 347f107c-b1a9-4dda-9087-6d242f2e18f0
- SPL ID
- 45c70020-828d-d6dd-e063-6394a90a8433
- Version
- 14
- Effective date
- 2025-12-12
- Source export date
- 2026-10-30
- 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/2026-10-30/9abf0f8b126f8aad070e21ea702bfb5e39ce670b16ae57dd52e8877705d1bf5d/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 19:28:08
| 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 | 205712 | derived:openfda.application_number |
| application number | NDA205712 | openfda.application_number | |
| brand name | Oxygen | openfda.brand_name | |
| generic name | OXYGEN | openfda.generic_name | |
| manufacturer name | SYOXSA, Inc. | openfda.manufacturer_name | |
| ndc | package | 23647-001-12 | openfda.package_ndc |
| ndc | package | 23647-001-15 | openfda.package_ndc |
| ndc | package | 23647-001-19 | openfda.package_ndc |
| ndc | package | 23647-001-11 | openfda.package_ndc |
| ndc | package | 23647-001-05 | openfda.package_ndc |
| ndc | package | 23647-001-03 | openfda.package_ndc |
| ndc | package | 23647-001-14 | openfda.package_ndc |
| ndc | package | 23647-001-18 | openfda.package_ndc |
| ndc | package | 23647-001-04 | openfda.package_ndc |
| ndc | package | 23647-001-02 | openfda.package_ndc |
| ndc | package | 23647-001-21 | openfda.package_ndc |
| ndc | package | 23647-001-08 | openfda.package_ndc |
| ndc | package | 23647-001-07 | openfda.package_ndc |
| ndc | package | 23647-001-16 | openfda.package_ndc |
| ndc | package | 23647-001-06 | openfda.package_ndc |
| ndc | package | 23647-001-01 | openfda.package_ndc |
| ndc | package | 23647-001-13 | openfda.package_ndc |
| ndc | package | 23647-001-09 | openfda.package_ndc |
| ndc | package | 23647-001-20 | openfda.package_ndc |
| ndc | package | 23647-001-10 | openfda.package_ndc |
| ndc | package | 23647-001-17 | openfda.package_ndc |
| ndc | product | 23647-001 | openfda.product_ndc |
| ndc11 | package | 23647000118 | derived:openfda.package_ndc |
| ndc11 | package | 23647000120 | derived:openfda.package_ndc |
| ndc11 | package | 23647000101 | derived:openfda.package_ndc |
| ndc11 | package | 23647000114 | derived:openfda.package_ndc |
| ndc11 | package | 23647000117 | derived:openfda.package_ndc |
| ndc11 | package | 23647000104 | derived:openfda.package_ndc |
| ndc11 | package | 23647000108 | derived:openfda.package_ndc |
| ndc11 | package | 23647000103 | derived:openfda.package_ndc |
| ndc11 | package | 23647000107 | derived:openfda.package_ndc |
| ndc11 | package | 23647000106 | derived:openfda.package_ndc |
| ndc11 | package | 23647000111 | derived:openfda.package_ndc |
| ndc11 | package | 23647000116 | derived:openfda.package_ndc |
| ndc11 | package | 23647000109 | derived:openfda.package_ndc |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.