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
- Aero All Gas Company
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- bd405eab-ac43-4590-975d-d0d1e8f78833
- SPL ID
- 423c874b-9b2a-21ee-e063-6294a90a5c17
- Version
- 16
- Effective date
- 2025-10-28
- Source export date
- 2026-09-28
- Source partition
- 5
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:34:16
| 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 | 206009 | derived:openfda.application_number |
| application number | NDA206009 | openfda.application_number | |
| brand name | Nitrous Oxide | openfda.brand_name | |
| generic name | NITROUS OXIDE | openfda.generic_name | |
| manufacturer name | Aero All Gas Company | openfda.manufacturer_name | |
| ndc | package | 10014-003-13 | openfda.package_ndc |
| ndc | package | 10014-003-14 | openfda.package_ndc |
| ndc | package | 10014-003-15 | openfda.package_ndc |
| ndc | package | 10014-003-11 | openfda.package_ndc |
| ndc | package | 10014-003-12 | openfda.package_ndc |
| ndc | package | 10014-003-10 | openfda.package_ndc |
| ndc | product | 10014-003 | openfda.product_ndc |
| ndc11 | package | 10014000314 | derived:openfda.package_ndc |
| ndc11 | package | 10014000312 | derived:openfda.package_ndc |
| ndc11 | package | 10014000310 | derived:openfda.package_ndc |
| ndc11 | package | 10014000311 | derived:openfda.package_ndc |
| ndc11 | package | 10014000313 | derived:openfda.package_ndc |
| ndc11 | package | 10014000315 | derived:openfda.package_ndc |
| rxcui | 312022 | openfda.rxcui | |
| spl id | 423c874b-9b2a-21ee-e063-6294a90a5c17 | id | |
| spl set id | bd405eab-ac43-4590-975d-d0d1e8f78833 | set_id | |
| unii | K50XQU1029 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.