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
- Boggs Gases div. Boggs Fire Equipment
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- d7eb457a-6cf5-c4d5-e053-2a95a90a90a3
- SPL ID
- 407fe0da-b50a-26bf-e063-6294a90a2df0
- Version
- 6
- Effective date
- 2025-10-06
- Source export date
- 2026-09-28
- Source partition
- 10
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:08:51
| 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 |
|---|---|---|---|
| brand name | Nitrous Oxide | openfda.brand_name | |
| generic name | NITROUS OXIDE | openfda.generic_name | |
| manufacturer name | Boggs Gases div. Boggs Fire Equipment | openfda.manufacturer_name | |
| ndc | package | 62097-0004-1 | openfda.package_ndc |
| ndc | package | 62097-0004-2 | openfda.package_ndc |
| ndc | package | 62097-0004-3 | openfda.package_ndc |
| ndc | product | 62097-0004 | openfda.product_ndc |
| ndc11 | package | 62097000403 | derived:openfda.package_ndc |
| ndc11 | package | 62097000401 | derived:openfda.package_ndc |
| ndc11 | package | 62097000402 | derived:openfda.package_ndc |
| rxcui | 312022 | openfda.rxcui | |
| spl id | 407fe0da-b50a-26bf-e063-6294a90a2df0 | id | |
| spl set id | d7eb457a-6cf5-c4d5-e053-2a95a90a90a3 | set_id | |
| unii | K50XQU1029 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.