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
- Machine & Welding Supply Company dba Arc3 Gases South
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- a5070767-c36a-4131-aa09-1bccfa24aa71
- SPL ID
- 44ff188e-3fdc-bfad-e063-6394a90a2ec6
- Version
- 18
- Effective date
- 2025-12-02
- Source export date
- 2026-09-28
- Source partition
- 4
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:25:33
| 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 | Machine & Welding Supply Company dba Arc3 Gases South | openfda.manufacturer_name | |
| ndc | package | 49575-003-06 | openfda.package_ndc |
| ndc | package | 49575-003-10 | openfda.package_ndc |
| ndc | package | 49575-003-14 | openfda.package_ndc |
| ndc | package | 49575-003-11 | openfda.package_ndc |
| ndc | package | 49575-003-13 | openfda.package_ndc |
| ndc | package | 49575-003-03 | openfda.package_ndc |
| ndc | package | 49575-003-08 | openfda.package_ndc |
| ndc | package | 49575-003-09 | openfda.package_ndc |
| ndc | package | 49575-003-02 | openfda.package_ndc |
| ndc | package | 49575-003-12 | openfda.package_ndc |
| ndc | package | 49575-003-04 | openfda.package_ndc |
| ndc | package | 49575-003-01 | openfda.package_ndc |
| ndc | product | 49575-003 | openfda.product_ndc |
| ndc11 | package | 49575000303 | derived:openfda.package_ndc |
| ndc11 | package | 49575000306 | derived:openfda.package_ndc |
| ndc11 | package | 49575000312 | derived:openfda.package_ndc |
| ndc11 | package | 49575000302 | derived:openfda.package_ndc |
| ndc11 | package | 49575000309 | derived:openfda.package_ndc |
| ndc11 | package | 49575000301 | derived:openfda.package_ndc |
| ndc11 | package | 49575000308 | derived:openfda.package_ndc |
| ndc11 | package | 49575000313 | derived:openfda.package_ndc |
| ndc11 | package | 49575000310 | derived:openfda.package_ndc |
| ndc11 | package | 49575000314 | derived:openfda.package_ndc |
| ndc11 | package | 49575000311 | derived:openfda.package_ndc |
| ndc11 | package | 49575000304 | derived:openfda.package_ndc |
| rxcui | 312022 | openfda.rxcui | |
| spl id | 44ff188e-3fdc-bfad-e063-6394a90a2ec6 | id | |
| spl set id | a5070767-c36a-4131-aa09-1bccfa24aa71 | set_id | |
| unii | K50XQU1029 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.