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
- Spectrum Gas Products, Inc
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- b550ebb2-e617-4913-8f75-1a07662e87e5
- SPL ID
- 450fd993-6aa5-df41-e063-6394a90aaef6
- Version
- 5
- Effective date
- 2025-12-03
- Source export date
- 2026-09-28
- Source partition
- 6
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:38:44
| 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 | Spectrum Gas Products, Inc | openfda.manufacturer_name | |
| ndc | package | 67525-400-03 | openfda.package_ndc |
| ndc | package | 67525-400-02 | openfda.package_ndc |
| ndc | package | 67525-400-04 | openfda.package_ndc |
| ndc | package | 67525-400-01 | openfda.package_ndc |
| ndc | product | 67525-400 | openfda.product_ndc |
| ndc11 | package | 67525040003 | derived:openfda.package_ndc |
| ndc11 | package | 67525040001 | derived:openfda.package_ndc |
| ndc11 | package | 67525040002 | derived:openfda.package_ndc |
| ndc11 | package | 67525040004 | derived:openfda.package_ndc |
| rxcui | 312022 | openfda.rxcui | |
| spl id | 450fd993-6aa5-df41-e063-6394a90aaef6 | id | |
| spl set id | b550ebb2-e617-4913-8f75-1a07662e87e5 | set_id | |
| unii | K50XQU1029 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.