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
- 2026-10-27
- 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/2026-10-27/35717de05250cd386420cc8ede3b6010b48d18eea2af59afb0617fcabca634ec/drug-label-0005-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 20:05:37
| 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.