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
- United States Welding, Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 8a791a86-caf1-4cdd-8c8d-235f8230a269
- SPL ID
- 1b6a6c96-28de-4721-8d0f-a80679772ca5
- Version
- 9
- Effective date
- 2024-10-29
- Source export date
- 2026-10-12
- Source partition
- 13
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 03:08:47
| 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 | 205704 | derived:openfda.application_number |
| application number | NDA205704 | openfda.application_number | |
| brand name | NITROUS OXIDE | openfda.brand_name | |
| generic name | NITROUS OXIDE | openfda.generic_name | |
| manufacturer name | United States Welding, Inc. | openfda.manufacturer_name | |
| ndc | package | 54218-800-02 | openfda.package_ndc |
| ndc | package | 54218-800-05 | openfda.package_ndc |
| ndc | package | 54218-800-01 | openfda.package_ndc |
| ndc | package | 54218-800-04 | openfda.package_ndc |
| ndc | package | 54218-800-03 | openfda.package_ndc |
| ndc | product | 54218-800 | openfda.product_ndc |
| ndc11 | package | 54218080004 | derived:openfda.package_ndc |
| ndc11 | package | 54218080002 | derived:openfda.package_ndc |
| ndc11 | package | 54218080001 | derived:openfda.package_ndc |
| ndc11 | package | 54218080005 | derived:openfda.package_ndc |
| ndc11 | package | 54218080003 | derived:openfda.package_ndc |
| rxcui | 312022 | openfda.rxcui | |
| spl id | 1b6a6c96-28de-4721-8d0f-a80679772ca5 | id | |
| spl set id | 8a791a86-caf1-4cdd-8c8d-235f8230a269 | set_id | |
| unii | K50XQU1029 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.