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
- Air Source Industries
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- eebd56c1-4ab3-409b-9767-e54dc42f2fce
- SPL ID
- c86cf8bb-09c3-434a-8514-2353f4f43d68
- Version
- 14
- Effective date
- 2024-10-06
- Source export date
- 2026-10-12
- 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/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:33:24
| 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 | Air Source Industries | openfda.manufacturer_name | |
| ndc | package | 10167-200-04 | openfda.package_ndc |
| ndc | package | 10167-200-09 | openfda.package_ndc |
| ndc | package | 10167-200-01 | openfda.package_ndc |
| ndc | package | 10167-200-08 | openfda.package_ndc |
| ndc | package | 10167-200-07 | openfda.package_ndc |
| ndc | package | 10167-200-11 | openfda.package_ndc |
| ndc | package | 10167-200-02 | openfda.package_ndc |
| ndc | package | 10167-200-10 | openfda.package_ndc |
| ndc | package | 10167-200-03 | openfda.package_ndc |
| ndc | package | 10167-200-05 | openfda.package_ndc |
| ndc | package | 10167-200-06 | openfda.package_ndc |
| ndc | product | 10167-200 | openfda.product_ndc |
| ndc11 | package | 10167020007 | derived:openfda.package_ndc |
| ndc11 | package | 10167020010 | derived:openfda.package_ndc |
| ndc11 | package | 10167020003 | derived:openfda.package_ndc |
| ndc11 | package | 10167020005 | derived:openfda.package_ndc |
| ndc11 | package | 10167020006 | derived:openfda.package_ndc |
| ndc11 | package | 10167020009 | derived:openfda.package_ndc |
| ndc11 | package | 10167020008 | derived:openfda.package_ndc |
| ndc11 | package | 10167020002 | derived:openfda.package_ndc |
| ndc11 | package | 10167020011 | derived:openfda.package_ndc |
| ndc11 | package | 10167020004 | derived:openfda.package_ndc |
| ndc11 | package | 10167020001 | derived:openfda.package_ndc |
| rxcui | 312022 | openfda.rxcui | |
| spl id | c86cf8bb-09c3-434a-8514-2353f4f43d68 | id | |
| spl set id | eebd56c1-4ab3-409b-9767-e54dc42f2fce | set_id | |
| unii | K50XQU1029 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.