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
- Gilmore Liquid Air Co.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 03fbd6e5-09a6-4f13-b251-63cf9ff129e9
- SPL ID
- 6af2649a-d5b6-4aee-99fe-2b252da914d8
- Version
- 10
- Effective date
- 2024-10-21
- Source export date
- 2026-10-12
- Source partition
- 6
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:47:47
| 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 | 205849 | derived:openfda.application_number |
| application number | NDA205849 | openfda.application_number | |
| brand name | OXYGEN | openfda.brand_name | |
| generic name | OXYGEN | openfda.generic_name | |
| manufacturer name | Gilmore Liquid Air Co. | openfda.manufacturer_name | |
| ndc | package | 51012-001-01 | openfda.package_ndc |
| ndc | package | 51012-001-03 | openfda.package_ndc |
| ndc | package | 51012-001-05 | openfda.package_ndc |
| ndc | package | 51012-001-10 | openfda.package_ndc |
| ndc | package | 51012-001-08 | openfda.package_ndc |
| ndc | package | 51012-001-02 | openfda.package_ndc |
| ndc | package | 51012-001-09 | openfda.package_ndc |
| ndc | package | 51012-001-04 | openfda.package_ndc |
| ndc | package | 51012-001-06 | openfda.package_ndc |
| ndc | package | 51012-001-07 | openfda.package_ndc |
| ndc | package | 51012-001-11 | openfda.package_ndc |
| ndc | product | 51012-001 | openfda.product_ndc |
| ndc11 | package | 51012000110 | derived:openfda.package_ndc |
| ndc11 | package | 51012000101 | derived:openfda.package_ndc |
| ndc11 | package | 51012000105 | derived:openfda.package_ndc |
| ndc11 | package | 51012000108 | derived:openfda.package_ndc |
| ndc11 | package | 51012000111 | derived:openfda.package_ndc |
| ndc11 | package | 51012000107 | derived:openfda.package_ndc |
| ndc11 | package | 51012000102 | derived:openfda.package_ndc |
| ndc11 | package | 51012000109 | derived:openfda.package_ndc |
| ndc11 | package | 51012000106 | derived:openfda.package_ndc |
| ndc11 | package | 51012000103 | derived:openfda.package_ndc |
| ndc11 | package | 51012000104 | derived:openfda.package_ndc |
| rxcui | 312172 | openfda.rxcui | |
| spl id | 6af2649a-d5b6-4aee-99fe-2b252da914d8 | id | |
| spl set id | 03fbd6e5-09a6-4f13-b251-63cf9ff129e9 | set_id | |
| unii | S88TT14065 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.