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
- American Welding & Gas
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 07aa2a86-d01e-470f-a12c-9908118bedc6
- SPL ID
- 5256f598-0209-1964-e063-6294a90aa4fa
- Version
- 19
- Effective date
- 2026-05-21
- Source export date
- 2026-09-28
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:27:35
| 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 | American Welding & Gas | openfda.manufacturer_name | |
| ndc | package | 44076-012-01 | openfda.package_ndc |
| ndc | package | 44076-012-10 | openfda.package_ndc |
| ndc | package | 44076-012-09 | openfda.package_ndc |
| ndc | package | 44076-012-02 | openfda.package_ndc |
| ndc | package | 44076-012-11 | openfda.package_ndc |
| ndc | package | 44076-012-04 | openfda.package_ndc |
| ndc | package | 44076-012-06 | openfda.package_ndc |
| ndc | package | 44076-012-14 | openfda.package_ndc |
| ndc | package | 44076-012-08 | openfda.package_ndc |
| ndc | package | 44076-012-05 | openfda.package_ndc |
| ndc | package | 44076-012-13 | openfda.package_ndc |
| ndc | package | 44076-012-07 | openfda.package_ndc |
| ndc | package | 44076-012-12 | openfda.package_ndc |
| ndc | package | 44076-012-03 | openfda.package_ndc |
| ndc | product | 44076-012 | openfda.product_ndc |
| ndc11 | package | 44076001210 | derived:openfda.package_ndc |
| ndc11 | package | 44076001208 | derived:openfda.package_ndc |
| ndc11 | package | 44076001201 | derived:openfda.package_ndc |
| ndc11 | package | 44076001213 | derived:openfda.package_ndc |
| ndc11 | package | 44076001202 | derived:openfda.package_ndc |
| ndc11 | package | 44076001211 | derived:openfda.package_ndc |
| ndc11 | package | 44076001207 | derived:openfda.package_ndc |
| ndc11 | package | 44076001214 | derived:openfda.package_ndc |
| ndc11 | package | 44076001206 | derived:openfda.package_ndc |
| ndc11 | package | 44076001203 | derived:openfda.package_ndc |
| ndc11 | package | 44076001209 | derived:openfda.package_ndc |
| ndc11 | package | 44076001204 | derived:openfda.package_ndc |
| ndc11 | package | 44076001212 | derived:openfda.package_ndc |
| ndc11 | package | 44076001205 | derived:openfda.package_ndc |
| rxcui | 312022 | openfda.rxcui | |
| spl id | 5256f598-0209-1964-e063-6294a90aa4fa | id | |
| spl set id | 07aa2a86-d01e-470f-a12c-9908118bedc6 | set_id | |
| unii | K50XQU1029 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.