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
- Crumpton Welding Supply & Equipment, Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- dc1626de-673a-4135-a023-203360be3b83
- SPL ID
- 52a996e1-7b79-4f0d-b28c-6d463fb10b70
- Version
- 10
- Effective date
- 2024-10-15
- Source export date
- 2026-10-30
- 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/2026-10-30/3b4c9bc1c064560160661a043b9878894ba805e5e90f4733fb76824b6ba7ac42/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 19:21:51
| 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 |
|---|---|---|---|
| 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 | Crumpton Welding Supply & Equipment, Inc. | openfda.manufacturer_name | |
| ndc | package | 52568-002-03 | openfda.package_ndc |
| ndc | package | 52568-002-06 | openfda.package_ndc |
| ndc | package | 52568-002-01 | openfda.package_ndc |
| ndc | package | 52568-002-02 | openfda.package_ndc |
| ndc | package | 52568-002-05 | openfda.package_ndc |
| ndc | package | 52568-002-04 | openfda.package_ndc |
| ndc | product | 52568-002 | openfda.product_ndc |
| ndc11 | package | 52568000205 | derived:openfda.package_ndc |
| ndc11 | package | 52568000204 | derived:openfda.package_ndc |
| ndc11 | package | 52568000201 | derived:openfda.package_ndc |
| ndc11 | package | 52568000206 | derived:openfda.package_ndc |
| ndc11 | package | 52568000203 | derived:openfda.package_ndc |
| ndc11 | package | 52568000202 | derived:openfda.package_ndc |
| rxcui | 312022 | openfda.rxcui | |
| spl id | 52a996e1-7b79-4f0d-b28c-6d463fb10b70 | id | |
| spl set id | dc1626de-673a-4135-a023-203360be3b83 | set_id | |
| unii | K50XQU1029 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.