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
- Roberts Oxygen Company, Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 988190eb-1449-482c-8120-c1d1390e2442
- SPL ID
- 43cf24ff-e7f5-6b53-e063-6394a90a8008
- Version
- 12
- Effective date
- 2025-11-17
- Source export date
- 2026-10-27
- 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/2026-10-27/d7629e6f844435cfe6cb0cf8c5341c46775ea16c5af42c77a22a2ffe820a2cd2/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 19:49:47
| 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 | Roberts Oxygen Company, Inc. | openfda.manufacturer_name | |
| ndc | package | 46123-006-07 | openfda.package_ndc |
| ndc | package | 46123-006-11 | openfda.package_ndc |
| ndc | package | 46123-006-05 | openfda.package_ndc |
| ndc | package | 46123-006-06 | openfda.package_ndc |
| ndc | package | 46123-006-03 | openfda.package_ndc |
| ndc | package | 46123-006-08 | openfda.package_ndc |
| ndc | package | 46123-006-04 | openfda.package_ndc |
| ndc | package | 46123-006-02 | openfda.package_ndc |
| ndc | package | 46123-006-01 | openfda.package_ndc |
| ndc | package | 46123-006-09 | openfda.package_ndc |
| ndc | package | 46123-006-10 | openfda.package_ndc |
| ndc | product | 46123-006 | openfda.product_ndc |
| ndc11 | package | 46123000608 | derived:openfda.package_ndc |
| ndc11 | package | 46123000607 | derived:openfda.package_ndc |
| ndc11 | package | 46123000610 | derived:openfda.package_ndc |
| ndc11 | package | 46123000602 | derived:openfda.package_ndc |
| ndc11 | package | 46123000606 | derived:openfda.package_ndc |
| ndc11 | package | 46123000604 | derived:openfda.package_ndc |
| ndc11 | package | 46123000601 | derived:openfda.package_ndc |
| ndc11 | package | 46123000609 | derived:openfda.package_ndc |
| ndc11 | package | 46123000611 | derived:openfda.package_ndc |
| ndc11 | package | 46123000605 | derived:openfda.package_ndc |
| ndc11 | package | 46123000603 | derived:openfda.package_ndc |
| rxcui | 312022 | openfda.rxcui | |
| spl id | 43cf24ff-e7f5-6b53-e063-6394a90a8008 | id | |
| spl set id | 988190eb-1449-482c-8120-c1d1390e2442 | set_id | |
| unii | K50XQU1029 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.