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
- Roberts Oxygen Company, Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 2bea6354-93df-477b-e063-6294a90a8480
- SPL ID
- 43cebe21-6fe8-89d9-e063-6294a90a282b
- Version
- 3
- Effective date
- 2025-11-17
- 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 06:26:27
| 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 | Roberts Oxygen Company, Inc. | openfda.manufacturer_name | |
| ndc | package | 46123-240-01 | openfda.package_ndc |
| ndc | package | 46123-240-02 | openfda.package_ndc |
| ndc | product | 46123-240 | openfda.product_ndc |
| ndc11 | package | 46123024002 | derived:openfda.package_ndc |
| ndc11 | package | 46123024001 | derived:openfda.package_ndc |
| rxcui | 309004 | openfda.rxcui | |
| spl id | 43cebe21-6fe8-89d9-e063-6294a90a282b | id | |
| spl set id | 2bea6354-93df-477b-e063-6294a90a8480 | set_id | |
| unii | 142M471B3J | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.