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
- O2 for U, Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 7e071898-47e7-6b92-e053-2a91aa0aff92
- SPL ID
- 4745a78f-5926-3702-e063-6394a90ad4f7
- Version
- 8
- Effective date
- 2025-12-31
- Source export date
- 2026-10-12
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:13:01
| 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 | O2 for U, Inc. | openfda.manufacturer_name | |
| ndc | package | 20175-072-20 | openfda.package_ndc |
| ndc | package | 20175-072-02 | openfda.package_ndc |
| ndc | package | 20175-072-12 | openfda.package_ndc |
| ndc | package | 20175-072-10 | openfda.package_ndc |
| ndc | package | 20175-072-09 | openfda.package_ndc |
| ndc | package | 20175-072-03 | openfda.package_ndc |
| ndc | package | 20175-072-05 | openfda.package_ndc |
| ndc | package | 20175-072-18 | openfda.package_ndc |
| ndc | package | 20175-072-01 | openfda.package_ndc |
| ndc | package | 20175-072-13 | openfda.package_ndc |
| ndc | package | 20175-072-17 | openfda.package_ndc |
| ndc | package | 20175-072-16 | openfda.package_ndc |
| ndc | package | 20175-072-14 | openfda.package_ndc |
| ndc | package | 20175-072-11 | openfda.package_ndc |
| ndc | package | 20175-072-08 | openfda.package_ndc |
| ndc | package | 20175-072-07 | openfda.package_ndc |
| ndc | package | 20175-072-15 | openfda.package_ndc |
| ndc | package | 20175-072-06 | openfda.package_ndc |
| ndc | package | 20175-072-04 | openfda.package_ndc |
| ndc | package | 20175-072-19 | openfda.package_ndc |
| ndc | product | 20175-072 | openfda.product_ndc |
| ndc11 | package | 20175007209 | derived:openfda.package_ndc |
| ndc11 | package | 20175007218 | derived:openfda.package_ndc |
| ndc11 | package | 20175007213 | derived:openfda.package_ndc |
| ndc11 | package | 20175007210 | derived:openfda.package_ndc |
| ndc11 | package | 20175007212 | derived:openfda.package_ndc |
| ndc11 | package | 20175007208 | derived:openfda.package_ndc |
| ndc11 | package | 20175007217 | derived:openfda.package_ndc |
| ndc11 | package | 20175007220 | derived:openfda.package_ndc |
| ndc11 | package | 20175007211 | derived:openfda.package_ndc |
| ndc11 | package | 20175007201 | derived:openfda.package_ndc |
| ndc11 | package | 20175007215 | derived:openfda.package_ndc |
| ndc11 | package | 20175007204 | derived:openfda.package_ndc |
| ndc11 | package | 20175007207 | derived:openfda.package_ndc |
| ndc11 | package | 20175007205 | derived:openfda.package_ndc |
| ndc11 | package | 20175007206 | derived:openfda.package_ndc |
| ndc11 | package | 20175007203 | derived:openfda.package_ndc |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.