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
- Oxarc, LLC
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 56d37fcb-8abf-4671-9388-a8837c94e5a2
- SPL ID
- 4475d50c-af27-b545-e063-6294a90a6b20
- Version
- 17
- Effective date
- 2025-11-25
- Source export date
- 2026-10-30
- 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/2026-10-30/e1583c3c823c7746dc6fefae78ac97d01bb558f7b0936fc3b7d2e673d3319207/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 18:34:41
| 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 | Oxarc, LLC | openfda.manufacturer_name | |
| ndc | package | 34057-010-05 | openfda.package_ndc |
| ndc | package | 34057-010-04 | openfda.package_ndc |
| ndc | package | 34057-010-03 | openfda.package_ndc |
| ndc | package | 34057-010-01 | openfda.package_ndc |
| ndc | package | 34057-010-02 | openfda.package_ndc |
| ndc | package | 34057-010-06 | openfda.package_ndc |
| ndc | product | 34057-010 | openfda.product_ndc |
| ndc11 | package | 34057001001 | derived:openfda.package_ndc |
| ndc11 | package | 34057001003 | derived:openfda.package_ndc |
| ndc11 | package | 34057001006 | derived:openfda.package_ndc |
| ndc11 | package | 34057001005 | derived:openfda.package_ndc |
| ndc11 | package | 34057001002 | derived:openfda.package_ndc |
| ndc11 | package | 34057001004 | derived:openfda.package_ndc |
| rxcui | 312022 | openfda.rxcui | |
| spl id | 4475d50c-af27-b545-e063-6294a90a6b20 | id | |
| spl set id | 56d37fcb-8abf-4671-9388-a8837c94e5a2 | set_id | |
| unii | K50XQU1029 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.