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
- General Air Service & Supply Co.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 2fd1831a-248d-4adc-8375-a08969d181e2
- SPL ID
- 4487592e-057a-9af8-e063-6394a90adf1d
- Version
- 20
- Effective date
- 2025-11-26
- Source export date
- 2026-09-28
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:46:25
| 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 | 207166 | derived:openfda.application_number |
| application number | NDA207166 | openfda.application_number | |
| brand name | Carbon Dioxide | openfda.brand_name | |
| generic name | CARBON DIOXIDE | openfda.generic_name | |
| manufacturer name | General Air Service & Supply Co. | openfda.manufacturer_name | |
| ndc | package | 21220-123-09 | openfda.package_ndc |
| ndc | package | 21220-123-08 | openfda.package_ndc |
| ndc | package | 21220-123-05 | openfda.package_ndc |
| ndc | package | 21220-123-01 | openfda.package_ndc |
| ndc | package | 21220-123-11 | openfda.package_ndc |
| ndc | package | 21220-123-10 | openfda.package_ndc |
| ndc | package | 21220-123-02 | openfda.package_ndc |
| ndc | package | 21220-123-04 | openfda.package_ndc |
| ndc | package | 21220-123-07 | openfda.package_ndc |
| ndc | package | 21220-123-03 | openfda.package_ndc |
| ndc | package | 21220-123-06 | openfda.package_ndc |
| ndc | product | 21220-123 | openfda.product_ndc |
| ndc11 | package | 21220012304 | derived:openfda.package_ndc |
| ndc11 | package | 21220012310 | derived:openfda.package_ndc |
| ndc11 | package | 21220012307 | derived:openfda.package_ndc |
| ndc11 | package | 21220012309 | derived:openfda.package_ndc |
| ndc11 | package | 21220012311 | derived:openfda.package_ndc |
| ndc11 | package | 21220012306 | derived:openfda.package_ndc |
| ndc11 | package | 21220012308 | derived:openfda.package_ndc |
| ndc11 | package | 21220012305 | derived:openfda.package_ndc |
| ndc11 | package | 21220012301 | derived:openfda.package_ndc |
| ndc11 | package | 21220012303 | derived:openfda.package_ndc |
| ndc11 | package | 21220012302 | derived:openfda.package_ndc |
| rxcui | 309004 | openfda.rxcui | |
| spl id | 4487592e-057a-9af8-e063-6394a90adf1d | id | |
| spl set id | 2fd1831a-248d-4adc-8375-a08969d181e2 | set_id | |
| unii | 142M471B3J | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.