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
- Arcet Equipment Company dba Arc3 Gases North
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- f0c5afcb-4e3c-44b6-9b20-409169a161aa
- SPL ID
- 471d36b6-5364-6b9e-e063-6294a90ad1e4
- Version
- 16
- Effective date
- 2025-12-29
- Source export date
- 2026-09-28
- 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/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:34:55
| 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 | 205712 | derived:openfda.application_number |
| application number | NDA205712 | openfda.application_number | |
| brand name | Oxygen | openfda.brand_name | |
| generic name | OXYGEN | openfda.generic_name | |
| manufacturer name | Arcet Equipment Company dba Arc3 Gases North | openfda.manufacturer_name | |
| ndc | package | 59788-001-32 | openfda.package_ndc |
| ndc | package | 59788-001-21 | openfda.package_ndc |
| ndc | package | 59788-001-10 | openfda.package_ndc |
| ndc | package | 59788-001-19 | openfda.package_ndc |
| ndc | package | 59788-001-24 | openfda.package_ndc |
| ndc | package | 59788-001-26 | openfda.package_ndc |
| ndc | package | 59788-001-25 | openfda.package_ndc |
| ndc | package | 59788-001-41 | openfda.package_ndc |
| ndc | package | 59788-001-40 | openfda.package_ndc |
| ndc | package | 59788-001-18 | openfda.package_ndc |
| ndc | package | 59788-001-27 | openfda.package_ndc |
| ndc | package | 59788-001-30 | openfda.package_ndc |
| ndc | package | 59788-001-36 | openfda.package_ndc |
| ndc | package | 59788-001-15 | openfda.package_ndc |
| ndc | package | 59788-001-33 | openfda.package_ndc |
| ndc | package | 59788-001-14 | openfda.package_ndc |
| ndc | package | 59788-001-17 | openfda.package_ndc |
| ndc | package | 59788-001-13 | openfda.package_ndc |
| ndc | package | 59788-001-34 | openfda.package_ndc |
| ndc | package | 59788-001-28 | openfda.package_ndc |
| ndc | package | 59788-001-20 | openfda.package_ndc |
| ndc | package | 59788-001-16 | openfda.package_ndc |
| ndc | package | 59788-001-23 | openfda.package_ndc |
| ndc | package | 59788-001-22 | openfda.package_ndc |
| ndc | package | 59788-001-29 | openfda.package_ndc |
| ndc | package | 59788-001-35 | openfda.package_ndc |
| ndc | package | 59788-001-42 | openfda.package_ndc |
| ndc | package | 59788-001-12 | openfda.package_ndc |
| ndc | package | 59788-001-31 | openfda.package_ndc |
| ndc | package | 59788-001-11 | openfda.package_ndc |
| ndc | product | 59788-001 | openfda.product_ndc |
| ndc11 | package | 59788000141 | derived:openfda.package_ndc |
| ndc11 | package | 59788000127 | derived:openfda.package_ndc |
| ndc11 | package | 59788000114 | derived:openfda.package_ndc |
| ndc11 | package | 59788000118 | derived:openfda.package_ndc |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.