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
- Airgas Usa, LLC
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 4e98dcd6-a01f-4b49-bc26-5e545a9faebe
- SPL ID
- a13020c5-5621-470c-ab24-89d73ea17c3e
- Version
- 8
- Effective date
- 2024-10-01
- Source export date
- 2026-10-12
- 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/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:58:36
| 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 | 206025 | derived:openfda.application_number |
| application number | NDA206025 | openfda.application_number | |
| brand name | Carbon Dioxide | openfda.brand_name | |
| generic name | CARBON DIOXIDE | openfda.generic_name | |
| manufacturer name | Airgas Usa, LLC | openfda.manufacturer_name | |
| ndc | package | 11054-021-01 | openfda.package_ndc |
| ndc | package | 11054-021-02 | openfda.package_ndc |
| ndc | product | 11054-021 | openfda.product_ndc |
| ndc11 | package | 11054002102 | derived:openfda.package_ndc |
| ndc11 | package | 11054002101 | derived:openfda.package_ndc |
| rxcui | 308998 | openfda.rxcui | |
| spl id | a13020c5-5621-470c-ab24-89d73ea17c3e | id | |
| spl set id | 4e98dcd6-a01f-4b49-bc26-5e545a9faebe | set_id | |
| unii | 142M471B3J | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.