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
- Pure-Ox, LLC
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 81691365-6b04-549a-e053-2a91aa0a0555
- SPL ID
- 57a2c6bb-dd3b-9161-e063-6394a90a4488
- Version
- 12
- Effective date
- 2026-07-27
- Source export date
- 2026-10-30
- 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/2026-10-30/3b4c9bc1c064560160661a043b9878894ba805e5e90f4733fb76824b6ba7ac42/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 19:20:26
| 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 | Pure-Ox, LLC | openfda.manufacturer_name | |
| ndc | package | 75828-001-06 | openfda.package_ndc |
| ndc | package | 75828-001-12 | openfda.package_ndc |
| ndc | package | 75828-001-10 | openfda.package_ndc |
| ndc | package | 75828-001-04 | openfda.package_ndc |
| ndc | package | 75828-001-05 | openfda.package_ndc |
| ndc | package | 75828-001-02 | openfda.package_ndc |
| ndc | package | 75828-001-09 | openfda.package_ndc |
| ndc | package | 75828-001-03 | openfda.package_ndc |
| ndc | package | 75828-001-11 | openfda.package_ndc |
| ndc | package | 75828-001-08 | openfda.package_ndc |
| ndc | package | 75828-001-07 | openfda.package_ndc |
| ndc | package | 75828-001-01 | openfda.package_ndc |
| ndc | product | 75828-001 | openfda.product_ndc |
| ndc11 | package | 75828000103 | derived:openfda.package_ndc |
| ndc11 | package | 75828000102 | derived:openfda.package_ndc |
| ndc11 | package | 75828000112 | derived:openfda.package_ndc |
| ndc11 | package | 75828000108 | derived:openfda.package_ndc |
| ndc11 | package | 75828000104 | derived:openfda.package_ndc |
| ndc11 | package | 75828000107 | derived:openfda.package_ndc |
| ndc11 | package | 75828000105 | derived:openfda.package_ndc |
| ndc11 | package | 75828000110 | derived:openfda.package_ndc |
| ndc11 | package | 75828000106 | derived:openfda.package_ndc |
| ndc11 | package | 75828000101 | derived:openfda.package_ndc |
| ndc11 | package | 75828000109 | derived:openfda.package_ndc |
| ndc11 | package | 75828000111 | derived:openfda.package_ndc |
| rxcui | 312172 | openfda.rxcui | |
| spl id | 57a2c6bb-dd3b-9161-e063-6394a90a4488 | id | |
| spl set id | 81691365-6b04-549a-e053-2a91aa0a0555 | set_id | |
| unii | S88TT14065 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.