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
- ILMO Products Company
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- bc5b4097-9292-41a2-82bb-30671b9ecf42
- SPL ID
- 424c9dbb-3e1d-e00f-e063-6294a90a74b2
- Version
- 16
- Effective date
- 2025-10-29
- 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 | ILMO Products Company | openfda.manufacturer_name | |
| ndc | package | 51486-007-06 | openfda.package_ndc |
| ndc | package | 51486-007-04 | openfda.package_ndc |
| ndc | package | 51486-007-03 | openfda.package_ndc |
| ndc | package | 51486-007-08 | openfda.package_ndc |
| ndc | package | 51486-007-05 | openfda.package_ndc |
| ndc | package | 51486-007-07 | openfda.package_ndc |
| ndc | package | 51486-007-01 | openfda.package_ndc |
| ndc | package | 51486-007-02 | openfda.package_ndc |
| ndc | product | 51486-007 | openfda.product_ndc |
| ndc11 | package | 51486000703 | derived:openfda.package_ndc |
| ndc11 | package | 51486000706 | derived:openfda.package_ndc |
| ndc11 | package | 51486000707 | derived:openfda.package_ndc |
| ndc11 | package | 51486000701 | derived:openfda.package_ndc |
| ndc11 | package | 51486000704 | derived:openfda.package_ndc |
| ndc11 | package | 51486000702 | derived:openfda.package_ndc |
| ndc11 | package | 51486000708 | derived:openfda.package_ndc |
| ndc11 | package | 51486000705 | derived:openfda.package_ndc |
| rxcui | 312022 | openfda.rxcui | |
| spl id | 424c9dbb-3e1d-e00f-e063-6294a90a74b2 | id | |
| spl set id | bc5b4097-9292-41a2-82bb-30671b9ecf42 | set_id | |
| unii | K50XQU1029 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.