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
- Westair Gases & Equipment, Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- ec885e73-b328-4bbb-90bf-728ec9517ad7
- SPL ID
- 4487d01b-70d3-2154-e063-6394a90ad85e
- Version
- 15
- Effective date
- 2025-11-26
- Source export date
- 2026-09-28
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:20:28
| 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 | Westair Gases & Equipment, Inc. | openfda.manufacturer_name | |
| ndc | package | 53440-003-02 | openfda.package_ndc |
| ndc | package | 53440-003-07 | openfda.package_ndc |
| ndc | package | 53440-003-01 | openfda.package_ndc |
| ndc | package | 53440-003-06 | openfda.package_ndc |
| ndc | package | 53440-003-09 | openfda.package_ndc |
| ndc | package | 53440-003-05 | openfda.package_ndc |
| ndc | package | 53440-003-03 | openfda.package_ndc |
| ndc | package | 53440-003-08 | openfda.package_ndc |
| ndc | package | 53440-003-04 | openfda.package_ndc |
| ndc | product | 53440-003 | openfda.product_ndc |
| ndc11 | package | 53440000303 | derived:openfda.package_ndc |
| ndc11 | package | 53440000301 | derived:openfda.package_ndc |
| ndc11 | package | 53440000309 | derived:openfda.package_ndc |
| ndc11 | package | 53440000305 | derived:openfda.package_ndc |
| ndc11 | package | 53440000302 | derived:openfda.package_ndc |
| ndc11 | package | 53440000306 | derived:openfda.package_ndc |
| ndc11 | package | 53440000308 | derived:openfda.package_ndc |
| ndc11 | package | 53440000304 | derived:openfda.package_ndc |
| ndc11 | package | 53440000307 | derived:openfda.package_ndc |
| rxcui | 347046 | openfda.rxcui | |
| spl id | 4487d01b-70d3-2154-e063-6394a90ad85e | id | |
| spl set id | ec885e73-b328-4bbb-90bf-728ec9517ad7 | set_id | |
| unii | K50XQU1029 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.