Nitrous Oxide
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
- Nitrous Oxide
- Generic name
- NITROUS OXIDE
- Manufacturer
- Metro Welding Supply Corporation
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 8f95cb3b-195f-41df-8f96-6c11703612ef
- SPL ID
- 4197bcf7-a748-43ea-e063-6294a90a1886
- Version
- 17
- Effective date
- 2025-10-20
- Source export date
- 2026-09-28
- Source partition
- 4
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:25:26
| 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 | 205704 | derived:openfda.application_number |
| application number | NDA205704 | openfda.application_number | |
| brand name | Nitrous Oxide | openfda.brand_name | |
| generic name | NITROUS OXIDE | openfda.generic_name | |
| manufacturer name | Metro Welding Supply Corporation | openfda.manufacturer_name | |
| ndc | package | 62273-005-02 | openfda.package_ndc |
| ndc | package | 62273-005-04 | openfda.package_ndc |
| ndc | package | 62273-005-01 | openfda.package_ndc |
| ndc | package | 62273-005-07 | openfda.package_ndc |
| ndc | package | 62273-005-05 | openfda.package_ndc |
| ndc | package | 62273-005-06 | openfda.package_ndc |
| ndc | package | 62273-005-03 | openfda.package_ndc |
| ndc | product | 62273-005 | openfda.product_ndc |
| ndc11 | package | 62273000502 | derived:openfda.package_ndc |
| ndc11 | package | 62273000505 | derived:openfda.package_ndc |
| ndc11 | package | 62273000503 | derived:openfda.package_ndc |
| ndc11 | package | 62273000504 | derived:openfda.package_ndc |
| ndc11 | package | 62273000507 | derived:openfda.package_ndc |
| ndc11 | package | 62273000501 | derived:openfda.package_ndc |
| ndc11 | package | 62273000506 | derived:openfda.package_ndc |
| rxcui | 312022 | openfda.rxcui | |
| spl id | 4197bcf7-a748-43ea-e063-6294a90a1886 | id | |
| spl set id | 8f95cb3b-195f-41df-8f96-6c11703612ef | set_id | |
| unii | K50XQU1029 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.