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
- Keen Compressed Gas Co. Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- cdefd579-5acb-45e0-a743-61426a7d2615
- SPL ID
- 43d1a2eb-7ea2-2816-e063-6294a90a34b8
- Version
- 14
- Effective date
- 2025-11-17
- Source export date
- 2026-09-28
- Source partition
- 13
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:38:10
| 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 | 206009 | derived:openfda.application_number |
| application number | NDA206009 | openfda.application_number | |
| brand name | NITROUS OXIDE | openfda.brand_name | |
| generic name | NITROUS OXIDE | openfda.generic_name | |
| manufacturer name | Keen Compressed Gas Co. Inc. | openfda.manufacturer_name | |
| ndc | package | 48273-002-04 | openfda.package_ndc |
| ndc | package | 48273-002-07 | openfda.package_ndc |
| ndc | package | 48273-002-05 | openfda.package_ndc |
| ndc | package | 48273-002-06 | openfda.package_ndc |
| ndc | package | 48273-002-09 | openfda.package_ndc |
| ndc | package | 48273-002-08 | openfda.package_ndc |
| ndc | product | 48273-002 | openfda.product_ndc |
| ndc11 | package | 48273000208 | derived:openfda.package_ndc |
| ndc11 | package | 48273000204 | derived:openfda.package_ndc |
| ndc11 | package | 48273000207 | derived:openfda.package_ndc |
| ndc11 | package | 48273000209 | derived:openfda.package_ndc |
| ndc11 | package | 48273000206 | derived:openfda.package_ndc |
| ndc11 | package | 48273000205 | derived:openfda.package_ndc |
| rxcui | 312022 | openfda.rxcui | |
| spl id | 43d1a2eb-7ea2-2816-e063-6294a90a34b8 | id | |
| spl set id | cdefd579-5acb-45e0-a743-61426a7d2615 | set_id | |
| unii | K50XQU1029 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.