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
- NEXAIR, LLC
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- a6f744e1-d94d-49e1-ab9f-9a88f04f5499
- SPL ID
- 52588e75-ec07-e529-e063-6294a90a1af8
- Version
- 20
- Effective date
- 2026-05-21
- Source export date
- 2026-10-27
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/977776a6cc37ec1c77259da8a93ae161850a3aa120341096e5a03428b84d016b/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 20:59:31
| 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 | NEXAIR, LLC | openfda.manufacturer_name | |
| ndc | package | 12213-593-21 | openfda.package_ndc |
| ndc | package | 12213-593-28 | openfda.package_ndc |
| ndc | package | 12213-593-58 | openfda.package_ndc |
| ndc | package | 12213-593-16 | openfda.package_ndc |
| ndc | package | 12213-593-14 | openfda.package_ndc |
| ndc | package | 12213-593-25 | openfda.package_ndc |
| ndc | package | 12213-593-24 | openfda.package_ndc |
| ndc | package | 12213-593-12 | openfda.package_ndc |
| ndc | package | 12213-593-23 | openfda.package_ndc |
| ndc | package | 12213-593-11 | openfda.package_ndc |
| ndc | package | 12213-593-37 | openfda.package_ndc |
| ndc | package | 12213-593-13 | openfda.package_ndc |
| ndc | package | 12213-593-15 | openfda.package_ndc |
| ndc | package | 12213-593-18 | openfda.package_ndc |
| ndc | package | 12213-593-19 | openfda.package_ndc |
| ndc | package | 12213-593-20 | openfda.package_ndc |
| ndc | package | 12213-593-17 | openfda.package_ndc |
| ndc | package | 12213-593-22 | openfda.package_ndc |
| ndc | product | 12213-593 | openfda.product_ndc |
| ndc11 | package | 12213059316 | derived:openfda.package_ndc |
| ndc11 | package | 12213059321 | derived:openfda.package_ndc |
| ndc11 | package | 12213059313 | derived:openfda.package_ndc |
| ndc11 | package | 12213059337 | derived:openfda.package_ndc |
| ndc11 | package | 12213059358 | derived:openfda.package_ndc |
| ndc11 | package | 12213059314 | derived:openfda.package_ndc |
| ndc11 | package | 12213059312 | derived:openfda.package_ndc |
| ndc11 | package | 12213059317 | derived:openfda.package_ndc |
| ndc11 | package | 12213059319 | derived:openfda.package_ndc |
| ndc11 | package | 12213059320 | derived:openfda.package_ndc |
| ndc11 | package | 12213059315 | derived:openfda.package_ndc |
| ndc11 | package | 12213059324 | derived:openfda.package_ndc |
| ndc11 | package | 12213059311 | derived:openfda.package_ndc |
| ndc11 | package | 12213059318 | derived:openfda.package_ndc |
| ndc11 | package | 12213059322 | derived:openfda.package_ndc |
| ndc11 | package | 12213059325 | derived:openfda.package_ndc |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.