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
- DJB Gas Services, Inc
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 403d8fa6-0c7a-4b87-a654-e0bb39c14327
- SPL ID
- 44713b93-5146-fa19-e063-6294a90a6cbd
- Version
- 18
- Effective date
- 2025-11-25
- Source export date
- 2026-11-06
- Source partition
- 9
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/423686b2ac39507df6931677ae004637f2f017f82cbe44b047a75ba358b9d453/drug-label-0009-of-0014.json.zip
- Source manifest SHA-256
- 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
- Import run
- 20261106T075659Z
- Imported at
- 2026-11-06 08:58:55
| 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 | 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 | DJB Gas Services, Inc | openfda.manufacturer_name | |
| ndc | package | 43621-003-21 | openfda.package_ndc |
| ndc | package | 43621-003-17 | openfda.package_ndc |
| ndc | package | 43621-003-13 | openfda.package_ndc |
| ndc | package | 43621-003-19 | openfda.package_ndc |
| ndc | package | 43621-003-14 | openfda.package_ndc |
| ndc | package | 43621-003-18 | openfda.package_ndc |
| ndc | package | 43621-003-15 | openfda.package_ndc |
| ndc | package | 43621-003-12 | openfda.package_ndc |
| ndc | package | 43621-003-20 | openfda.package_ndc |
| ndc | package | 43621-003-11 | openfda.package_ndc |
| ndc | package | 43621-003-16 | openfda.package_ndc |
| ndc | product | 43621-003 | openfda.product_ndc |
| ndc11 | package | 43621000319 | derived:openfda.package_ndc |
| ndc11 | package | 43621000312 | derived:openfda.package_ndc |
| ndc11 | package | 43621000314 | derived:openfda.package_ndc |
| ndc11 | package | 43621000320 | derived:openfda.package_ndc |
| ndc11 | package | 43621000311 | derived:openfda.package_ndc |
| ndc11 | package | 43621000313 | derived:openfda.package_ndc |
| ndc11 | package | 43621000316 | derived:openfda.package_ndc |
| ndc11 | package | 43621000315 | derived:openfda.package_ndc |
| ndc11 | package | 43621000321 | derived:openfda.package_ndc |
| ndc11 | package | 43621000318 | derived:openfda.package_ndc |
| ndc11 | package | 43621000317 | derived:openfda.package_ndc |
| rxcui | 312022 | openfda.rxcui | |
| spl id | 44713b93-5146-fa19-e063-6294a90a6cbd | id | |
| spl set id | 403d8fa6-0c7a-4b87-a654-e0bb39c14327 | set_id | |
| unii | K50XQU1029 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.