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
- Johnson Medical Consulting, Inc dba Combined Home Medical Equipment
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 7d511972-6358-4426-e053-2a91aa0a8732
- SPL ID
- 46a46e95-1dfd-3238-e063-6294a90a49eb
- Version
- 8
- Effective date
- 2025-12-23
- Source export date
- 2026-09-28
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:49:02
| 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 | Johnson Medical Consulting, Inc dba Combined Home Medical Equipment | openfda.manufacturer_name | |
| ndc | package | 66503-001-07 | openfda.package_ndc |
| ndc | package | 66503-001-01 | openfda.package_ndc |
| ndc | package | 66503-001-03 | openfda.package_ndc |
| ndc | package | 66503-001-04 | openfda.package_ndc |
| ndc | package | 66503-001-02 | openfda.package_ndc |
| ndc | package | 66503-001-08 | openfda.package_ndc |
| ndc | package | 66503-001-06 | openfda.package_ndc |
| ndc | package | 66503-001-05 | openfda.package_ndc |
| ndc | package | 66503-001-10 | openfda.package_ndc |
| ndc | package | 66503-001-09 | openfda.package_ndc |
| ndc | product | 66503-001 | openfda.product_ndc |
| ndc11 | package | 66503000104 | derived:openfda.package_ndc |
| ndc11 | package | 66503000108 | derived:openfda.package_ndc |
| ndc11 | package | 66503000107 | derived:openfda.package_ndc |
| ndc11 | package | 66503000106 | derived:openfda.package_ndc |
| ndc11 | package | 66503000101 | derived:openfda.package_ndc |
| ndc11 | package | 66503000109 | derived:openfda.package_ndc |
| ndc11 | package | 66503000102 | derived:openfda.package_ndc |
| ndc11 | package | 66503000110 | derived:openfda.package_ndc |
| ndc11 | package | 66503000105 | derived:openfda.package_ndc |
| ndc11 | package | 66503000103 | derived:openfda.package_ndc |
| rxcui | 312172 | openfda.rxcui | |
| spl id | 46a46e95-1dfd-3238-e063-6294a90a49eb | id | |
| spl set id | 7d511972-6358-4426-e053-2a91aa0a8732 | set_id | |
| unii | S88TT14065 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.