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
- General Welding Supply Corp.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- f39618a6-a387-44fe-b5f9-bbfedc95904b
- SPL ID
- 40819971-3c4d-cb6e-e063-6294a90a92f4
- Version
- 11
- Effective date
- 2025-10-06
- Source export date
- 2026-10-30
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-30/023bc8d8aae5addb7530087bbbdb169b3ccbf36764f15b8ca67db07e1e5aea8b/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 19:08:12
| 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 | General Welding Supply Corp. | openfda.manufacturer_name | |
| ndc | package | 20703-003-03 | openfda.package_ndc |
| ndc | package | 20703-003-02 | openfda.package_ndc |
| ndc | package | 20703-003-01 | openfda.package_ndc |
| ndc | product | 20703-003 | openfda.product_ndc |
| ndc11 | package | 20703000301 | derived:openfda.package_ndc |
| ndc11 | package | 20703000303 | derived:openfda.package_ndc |
| ndc11 | package | 20703000302 | derived:openfda.package_ndc |
| rxcui | 312022 | openfda.rxcui | |
| spl id | 40819971-3c4d-cb6e-e063-6294a90a92f4 | id | |
| spl set id | f39618a6-a387-44fe-b5f9-bbfedc95904b | set_id | |
| unii | K50XQU1029 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.