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
- Corrigan Propane LLC dba Blue Water Industrial Products
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- b02472d8-ee0f-4218-8693-0d7970532ce9
- SPL ID
- 9a0fbf8f-d083-44d7-9f08-5894f12e338e
- Version
- 9
- Effective date
- 2024-10-14
- Source export date
- 2026-10-12
- Source partition
- 9
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/fb14b8f3d34b45230a84f851c029385f512adf3f002423a9b78d4f7ca626ecec/drug-label-0009-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:25:40
| 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 | Corrigan Propane LLC dba Blue Water Industrial Products | openfda.manufacturer_name | |
| ndc | package | 44517-020-05 | openfda.package_ndc |
| ndc | package | 44517-020-07 | openfda.package_ndc |
| ndc | package | 44517-020-02 | openfda.package_ndc |
| ndc | package | 44517-020-06 | openfda.package_ndc |
| ndc | package | 44517-020-08 | openfda.package_ndc |
| ndc | package | 44517-020-04 | openfda.package_ndc |
| ndc | package | 44517-020-03 | openfda.package_ndc |
| ndc | package | 44517-020-01 | openfda.package_ndc |
| ndc | package | 44517-020-09 | openfda.package_ndc |
| ndc | product | 44517-020 | openfda.product_ndc |
| ndc11 | package | 44517002009 | derived:openfda.package_ndc |
| ndc11 | package | 44517002005 | derived:openfda.package_ndc |
| ndc11 | package | 44517002006 | derived:openfda.package_ndc |
| ndc11 | package | 44517002004 | derived:openfda.package_ndc |
| ndc11 | package | 44517002002 | derived:openfda.package_ndc |
| ndc11 | package | 44517002003 | derived:openfda.package_ndc |
| ndc11 | package | 44517002001 | derived:openfda.package_ndc |
| ndc11 | package | 44517002008 | derived:openfda.package_ndc |
| ndc11 | package | 44517002007 | derived:openfda.package_ndc |
| rxcui | 312022 | openfda.rxcui | |
| spl id | 9a0fbf8f-d083-44d7-9f08-5894f12e338e | id | |
| spl set id | b02472d8-ee0f-4218-8693-0d7970532ce9 | set_id | |
| unii | K50XQU1029 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.