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
- Air Source Industries Inc
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- fb06a622-e2d2-4dec-9fc4-65eec94978e4
- SPL ID
- ded7606b-a1bc-4be8-8809-918f125674a8
- Version
- 11
- Effective date
- 2024-10-06
- Source export date
- 2026-10-12
- Source partition
- 4
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:37:31
| 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 | Air Source Industries Inc | openfda.manufacturer_name | |
| ndc | package | 10167-500-03 | openfda.package_ndc |
| ndc | package | 10167-500-05 | openfda.package_ndc |
| ndc | package | 10167-500-06 | openfda.package_ndc |
| ndc | package | 10167-500-08 | openfda.package_ndc |
| ndc | package | 10167-500-01 | openfda.package_ndc |
| ndc | package | 10167-500-02 | openfda.package_ndc |
| ndc | package | 10167-500-07 | openfda.package_ndc |
| ndc | package | 10167-500-09 | openfda.package_ndc |
| ndc | package | 10167-500-04 | openfda.package_ndc |
| ndc | product | 10167-500 | openfda.product_ndc |
| ndc11 | package | 10167050002 | derived:openfda.package_ndc |
| ndc11 | package | 10167050005 | derived:openfda.package_ndc |
| ndc11 | package | 10167050003 | derived:openfda.package_ndc |
| ndc11 | package | 10167050006 | derived:openfda.package_ndc |
| ndc11 | package | 10167050001 | derived:openfda.package_ndc |
| ndc11 | package | 10167050004 | derived:openfda.package_ndc |
| ndc11 | package | 10167050009 | derived:openfda.package_ndc |
| ndc11 | package | 10167050008 | derived:openfda.package_ndc |
| ndc11 | package | 10167050007 | derived:openfda.package_ndc |
| rxcui | 309004 | openfda.rxcui | |
| spl id | ded7606b-a1bc-4be8-8809-918f125674a8 | id | |
| spl set id | fb06a622-e2d2-4dec-9fc4-65eec94978e4 | set_id | |
| unii | 142M471B3J | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.