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
- Dennis Welding Supply, Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 87e97409-cdd9-4b35-ab7a-d1c5f6f1d2e1
- SPL ID
- abe3c1c6-048a-4e02-94de-1a0a8f81e1a5
- Version
- 11
- Effective date
- 2025-12-12
- Source export date
- 2026-09-28
- Source partition
- 4
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:27:26
| 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 |
|---|---|---|---|
| brand name | OXYGEN | openfda.brand_name | |
| generic name | OXYGEN | openfda.generic_name | |
| manufacturer name | Dennis Welding Supply, Inc. | openfda.manufacturer_name | |
| ndc | package | 53720-001-04 | openfda.package_ndc |
| ndc | package | 53720-001-05 | openfda.package_ndc |
| ndc | package | 53720-001-02 | openfda.package_ndc |
| ndc | package | 53720-001-08 | openfda.package_ndc |
| ndc | package | 53720-001-01 | openfda.package_ndc |
| ndc | package | 53720-001-03 | openfda.package_ndc |
| ndc | package | 53720-001-07 | openfda.package_ndc |
| ndc | package | 53720-001-10 | openfda.package_ndc |
| ndc | package | 53720-001-09 | openfda.package_ndc |
| ndc | package | 53720-001-11 | openfda.package_ndc |
| ndc | package | 53720-001-06 | openfda.package_ndc |
| ndc | product | 53720-001 | openfda.product_ndc |
| ndc11 | package | 53720000106 | derived:openfda.package_ndc |
| ndc11 | package | 53720000108 | derived:openfda.package_ndc |
| ndc11 | package | 53720000102 | derived:openfda.package_ndc |
| ndc11 | package | 53720000104 | derived:openfda.package_ndc |
| ndc11 | package | 53720000103 | derived:openfda.package_ndc |
| ndc11 | package | 53720000111 | derived:openfda.package_ndc |
| ndc11 | package | 53720000107 | derived:openfda.package_ndc |
| ndc11 | package | 53720000101 | derived:openfda.package_ndc |
| ndc11 | package | 53720000105 | derived:openfda.package_ndc |
| ndc11 | package | 53720000109 | derived:openfda.package_ndc |
| ndc11 | package | 53720000110 | derived:openfda.package_ndc |
| rxcui | 312172 | openfda.rxcui | |
| spl id | abe3c1c6-048a-4e02-94de-1a0a8f81e1a5 | id | |
| spl set id | 87e97409-cdd9-4b35-ab7a-d1c5f6f1d2e1 | set_id | |
| unii | S88TT14065 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.