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
- Volunteer Welding Supply Inc
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 5c05dbd2-fd6b-462f-957a-b7ecf66ab27e
- SPL ID
- 44831b3a-2554-9e64-e063-6394a90a8722
- Version
- 11
- Effective date
- 2025-11-26
- Source export date
- 2026-09-28
- Source partition
- 6
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:34:34
| 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 | Volunteer Welding Supply Inc | openfda.manufacturer_name | |
| ndc | package | 53511-003-07 | openfda.package_ndc |
| ndc | package | 53511-003-01 | openfda.package_ndc |
| ndc | package | 53511-003-03 | openfda.package_ndc |
| ndc | package | 53511-003-02 | openfda.package_ndc |
| ndc | package | 53511-003-05 | openfda.package_ndc |
| ndc | package | 53511-003-06 | openfda.package_ndc |
| ndc | package | 53511-003-04 | openfda.package_ndc |
| ndc | product | 53511-003 | openfda.product_ndc |
| ndc11 | package | 53511000302 | derived:openfda.package_ndc |
| ndc11 | package | 53511000301 | derived:openfda.package_ndc |
| ndc11 | package | 53511000303 | derived:openfda.package_ndc |
| ndc11 | package | 53511000307 | derived:openfda.package_ndc |
| ndc11 | package | 53511000306 | derived:openfda.package_ndc |
| ndc11 | package | 53511000305 | derived:openfda.package_ndc |
| ndc11 | package | 53511000304 | derived:openfda.package_ndc |
| rxcui | 312022 | openfda.rxcui | |
| spl id | 44831b3a-2554-9e64-e063-6394a90a8722 | id | |
| spl set id | 5c05dbd2-fd6b-462f-957a-b7ecf66ab27e | set_id | |
| unii | K50XQU1029 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.