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
- Red Ball Oxygen Co., Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 02a3cf7f-d0a5-4edd-bc84-d9162558434b
- SPL ID
- 4a2f48b9-8be5-327c-e063-6294a90ad295
- Version
- 21
- Effective date
- 2026-02-06
- Source export date
- 2026-10-30
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-30/0b630a6825fc0c8abba22d7c8fd4d069bde78bef928766047ddbb369119f337f/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 18:59:08
| 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 | Red Ball Oxygen Co., Inc. | openfda.manufacturer_name | |
| ndc | package | 46362-003-07 | openfda.package_ndc |
| ndc | package | 46362-003-04 | openfda.package_ndc |
| ndc | package | 46362-003-06 | openfda.package_ndc |
| ndc | package | 46362-003-02 | openfda.package_ndc |
| ndc | package | 46362-003-05 | openfda.package_ndc |
| ndc | package | 46362-003-01 | openfda.package_ndc |
| ndc | package | 46362-003-03 | openfda.package_ndc |
| ndc | product | 46362-003 | openfda.product_ndc |
| ndc11 | package | 46362000305 | derived:openfda.package_ndc |
| ndc11 | package | 46362000306 | derived:openfda.package_ndc |
| ndc11 | package | 46362000303 | derived:openfda.package_ndc |
| ndc11 | package | 46362000301 | derived:openfda.package_ndc |
| ndc11 | package | 46362000304 | derived:openfda.package_ndc |
| ndc11 | package | 46362000307 | derived:openfda.package_ndc |
| ndc11 | package | 46362000302 | derived:openfda.package_ndc |
| rxcui | 347166 | openfda.rxcui | |
| spl id | 4a2f48b9-8be5-327c-e063-6294a90ad295 | id | |
| spl set id | 02a3cf7f-d0a5-4edd-bc84-d9162558434b | set_id | |
| unii | K50XQU1029 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.