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
- WSM SUPPLIER LLC.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 17e334cc-a3af-d4f0-e063-6294a90ae41e
- SPL ID
- 40a9f90f-59ef-d5ca-e063-6294a90abc91
- Version
- 3
- Effective date
- 2025-10-08
- Source export date
- 2026-10-30
- Source partition
- 13
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-30/8d15bdc5962e7531569eaeb5b1b2e4919574d40a6782ab67345a27b890175a00/drug-label-0013-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 19:58:28
| 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 | 209989 | derived:openfda.application_number |
| application number | NDA209989 | openfda.application_number | |
| brand name | Nitrous Oxide | openfda.brand_name | |
| generic name | NITROUS OXIDE | openfda.generic_name | |
| manufacturer name | WSM SUPPLIER LLC. | openfda.manufacturer_name | |
| ndc | package | 84120-003-01 | openfda.package_ndc |
| ndc | package | 84120-003-13 | openfda.package_ndc |
| ndc | package | 84120-003-04 | openfda.package_ndc |
| ndc | package | 84120-003-02 | openfda.package_ndc |
| ndc | package | 84120-003-03 | openfda.package_ndc |
| ndc | package | 84120-003-09 | openfda.package_ndc |
| ndc | package | 84120-003-15 | openfda.package_ndc |
| ndc | package | 84120-003-08 | openfda.package_ndc |
| ndc | package | 84120-003-07 | openfda.package_ndc |
| ndc | package | 84120-003-12 | openfda.package_ndc |
| ndc | package | 84120-003-10 | openfda.package_ndc |
| ndc | package | 84120-003-11 | openfda.package_ndc |
| ndc | package | 84120-003-05 | openfda.package_ndc |
| ndc | package | 84120-003-06 | openfda.package_ndc |
| ndc | package | 84120-003-14 | openfda.package_ndc |
| ndc | product | 84120-003 | openfda.product_ndc |
| ndc11 | package | 84120000302 | derived:openfda.package_ndc |
| ndc11 | package | 84120000313 | derived:openfda.package_ndc |
| ndc11 | package | 84120000311 | derived:openfda.package_ndc |
| ndc11 | package | 84120000303 | derived:openfda.package_ndc |
| ndc11 | package | 84120000312 | derived:openfda.package_ndc |
| ndc11 | package | 84120000304 | derived:openfda.package_ndc |
| ndc11 | package | 84120000314 | derived:openfda.package_ndc |
| ndc11 | package | 84120000310 | derived:openfda.package_ndc |
| ndc11 | package | 84120000306 | derived:openfda.package_ndc |
| ndc11 | package | 84120000315 | derived:openfda.package_ndc |
| ndc11 | package | 84120000301 | derived:openfda.package_ndc |
| ndc11 | package | 84120000305 | derived:openfda.package_ndc |
| ndc11 | package | 84120000307 | derived:openfda.package_ndc |
| ndc11 | package | 84120000308 | derived:openfda.package_ndc |
| ndc11 | package | 84120000309 | derived:openfda.package_ndc |
| rxcui | 347166 | openfda.rxcui | |
| spl id | 40a9f90f-59ef-d5ca-e063-6294a90abc91 | id | |
| spl set id | 17e334cc-a3af-d4f0-e063-6294a90ae41e | set_id | |
| unii | K50XQU1029 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.