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
- ADF Welding & Medical, Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 01efe36d-5281-4ede-bc30-9a1727a86a83
- SPL ID
- 91dd8a34-97b6-4d15-ac25-e864926dd978
- Version
- 12
- Effective date
- 2024-10-02
- Source export date
- 2026-09-28
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:29:45
| 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 | 205767 | derived:openfda.application_number |
| application number | NDA205767 | openfda.application_number | |
| brand name | Oxygen | openfda.brand_name | |
| generic name | OXYGEN | openfda.generic_name | |
| manufacturer name | ADF Welding & Medical, Inc. | openfda.manufacturer_name | |
| ndc | package | 64922-233-11 | openfda.package_ndc |
| ndc | package | 64922-233-04 | openfda.package_ndc |
| ndc | package | 64922-233-08 | openfda.package_ndc |
| ndc | package | 64922-233-06 | openfda.package_ndc |
| ndc | package | 64922-233-05 | openfda.package_ndc |
| ndc | package | 64922-233-01 | openfda.package_ndc |
| ndc | package | 64922-233-10 | openfda.package_ndc |
| ndc | package | 64922-233-09 | openfda.package_ndc |
| ndc | package | 64922-233-02 | openfda.package_ndc |
| ndc | package | 64922-233-03 | openfda.package_ndc |
| ndc | product | 64922-233 | openfda.product_ndc |
| ndc11 | package | 64922023308 | derived:openfda.package_ndc |
| ndc11 | package | 64922023309 | derived:openfda.package_ndc |
| ndc11 | package | 64922023311 | derived:openfda.package_ndc |
| ndc11 | package | 64922023310 | derived:openfda.package_ndc |
| ndc11 | package | 64922023301 | derived:openfda.package_ndc |
| ndc11 | package | 64922023304 | derived:openfda.package_ndc |
| ndc11 | package | 64922023305 | derived:openfda.package_ndc |
| ndc11 | package | 64922023303 | derived:openfda.package_ndc |
| ndc11 | package | 64922023302 | derived:openfda.package_ndc |
| ndc11 | package | 64922023306 | derived:openfda.package_ndc |
| rxcui | 312172 | openfda.rxcui | |
| spl id | 91dd8a34-97b6-4d15-ac25-e864926dd978 | id | |
| spl set id | 01efe36d-5281-4ede-bc30-9a1727a86a83 | set_id | |
| unii | S88TT14065 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.