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
- United States Welding, Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 59765eb8-b22d-4514-b208-058b18727fc5
- SPL ID
- 39eb6b47-d231-4d73-b1b4-509cc6ddf034
- Version
- 13
- Effective date
- 2024-10-29
- Source export date
- 2026-09-28
- 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/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:09:23
| 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 | United States Welding, Inc. | openfda.manufacturer_name | |
| ndc | package | 54218-500-08 | openfda.package_ndc |
| ndc | package | 54218-500-06 | openfda.package_ndc |
| ndc | package | 54218-500-17 | openfda.package_ndc |
| ndc | package | 54218-500-12 | openfda.package_ndc |
| ndc | package | 54218-500-21 | openfda.package_ndc |
| ndc | package | 54218-500-10 | openfda.package_ndc |
| ndc | package | 54218-500-20 | openfda.package_ndc |
| ndc | package | 54218-500-04 | openfda.package_ndc |
| ndc | package | 54218-500-19 | openfda.package_ndc |
| ndc | package | 54218-500-05 | openfda.package_ndc |
| ndc | package | 54218-500-18 | openfda.package_ndc |
| ndc | package | 54218-500-01 | openfda.package_ndc |
| ndc | package | 54218-500-09 | openfda.package_ndc |
| ndc | package | 54218-500-14 | openfda.package_ndc |
| ndc | package | 54218-500-02 | openfda.package_ndc |
| ndc | package | 54218-500-15 | openfda.package_ndc |
| ndc | package | 54218-500-16 | openfda.package_ndc |
| ndc | package | 54218-500-13 | openfda.package_ndc |
| ndc | package | 54218-500-11 | openfda.package_ndc |
| ndc | package | 54218-500-07 | openfda.package_ndc |
| ndc | package | 54218-500-03 | openfda.package_ndc |
| ndc | product | 54218-500 | openfda.product_ndc |
| ndc11 | package | 54218050019 | derived:openfda.package_ndc |
| ndc11 | package | 54218050008 | derived:openfda.package_ndc |
| ndc11 | package | 54218050001 | derived:openfda.package_ndc |
| ndc11 | package | 54218050013 | derived:openfda.package_ndc |
| ndc11 | package | 54218050016 | derived:openfda.package_ndc |
| ndc11 | package | 54218050003 | derived:openfda.package_ndc |
| ndc11 | package | 54218050007 | derived:openfda.package_ndc |
| ndc11 | package | 54218050004 | derived:openfda.package_ndc |
| ndc11 | package | 54218050018 | derived:openfda.package_ndc |
| ndc11 | package | 54218050015 | derived:openfda.package_ndc |
| ndc11 | package | 54218050002 | derived:openfda.package_ndc |
| ndc11 | package | 54218050005 | derived:openfda.package_ndc |
| ndc11 | package | 54218050017 | derived:openfda.package_ndc |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.