CARBON DIOXIDE
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
- CARBON DIOXIDE
- Generic name
- CARBON DIOXIDE
- Manufacturer
- Norco, Inc
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- d37f56ac-23e7-4d6e-af85-f26a712ccef9
- SPL ID
- 4601ddc9-ba98-9569-e063-6294a90a87f6
- Version
- 8
- Effective date
- 2025-12-15
- 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 06:26:37
| 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 | 205764 | derived:openfda.application_number |
| application number | NDA205764 | openfda.application_number | |
| brand name | CARBON DIOXIDE | openfda.brand_name | |
| generic name | CARBON DIOXIDE | openfda.generic_name | |
| manufacturer name | Norco, Inc | openfda.manufacturer_name | |
| ndc | package | 42602-006-06 | openfda.package_ndc |
| ndc | package | 42602-006-01 | openfda.package_ndc |
| ndc | package | 42602-006-05 | openfda.package_ndc |
| ndc | package | 42602-006-03 | openfda.package_ndc |
| ndc | package | 42602-006-02 | openfda.package_ndc |
| ndc | package | 42602-006-04 | openfda.package_ndc |
| ndc | package | 42602-006-07 | openfda.package_ndc |
| ndc | product | 42602-006 | openfda.product_ndc |
| ndc11 | package | 42602000607 | derived:openfda.package_ndc |
| ndc11 | package | 42602000603 | derived:openfda.package_ndc |
| ndc11 | package | 42602000604 | derived:openfda.package_ndc |
| ndc11 | package | 42602000605 | derived:openfda.package_ndc |
| ndc11 | package | 42602000606 | derived:openfda.package_ndc |
| ndc11 | package | 42602000602 | derived:openfda.package_ndc |
| ndc11 | package | 42602000601 | derived:openfda.package_ndc |
| rxcui | 309004 | openfda.rxcui | |
| spl id | 4601ddc9-ba98-9569-e063-6294a90a87f6 | id | |
| spl set id | d37f56ac-23e7-4d6e-af85-f26a712ccef9 | set_id | |
| unii | 142M471B3J | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.