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
- Westair Gases & Equipment, Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 81a70f82-9fa1-4751-b81f-1c622045634f
- SPL ID
- 4487ca09-1ab4-1181-e063-6394a90a4d46
- Version
- 16
- Effective date
- 2025-11-26
- Source export date
- 2026-09-28
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:14:48
| 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 | Westair Gases & Equipment, Inc. | openfda.manufacturer_name | |
| ndc | package | 53440-004-07 | openfda.package_ndc |
| ndc | package | 53440-004-03 | openfda.package_ndc |
| ndc | package | 53440-004-04 | openfda.package_ndc |
| ndc | package | 53440-004-15 | openfda.package_ndc |
| ndc | package | 53440-004-14 | openfda.package_ndc |
| ndc | package | 53440-004-11 | openfda.package_ndc |
| ndc | package | 53440-004-05 | openfda.package_ndc |
| ndc | package | 53440-004-01 | openfda.package_ndc |
| ndc | package | 53440-004-13 | openfda.package_ndc |
| ndc | package | 53440-004-16 | openfda.package_ndc |
| ndc | package | 53440-004-08 | openfda.package_ndc |
| ndc | package | 53440-004-02 | openfda.package_ndc |
| ndc | package | 53440-004-09 | openfda.package_ndc |
| ndc | package | 53440-004-17 | openfda.package_ndc |
| ndc | package | 53440-004-10 | openfda.package_ndc |
| ndc | package | 53440-004-06 | openfda.package_ndc |
| ndc | package | 53440-004-12 | openfda.package_ndc |
| ndc | product | 53440-004 | openfda.product_ndc |
| ndc11 | package | 53440000401 | derived:openfda.package_ndc |
| ndc11 | package | 53440000410 | derived:openfda.package_ndc |
| ndc11 | package | 53440000407 | derived:openfda.package_ndc |
| ndc11 | package | 53440000416 | derived:openfda.package_ndc |
| ndc11 | package | 53440000406 | derived:openfda.package_ndc |
| ndc11 | package | 53440000403 | derived:openfda.package_ndc |
| ndc11 | package | 53440000405 | derived:openfda.package_ndc |
| ndc11 | package | 53440000404 | derived:openfda.package_ndc |
| ndc11 | package | 53440000408 | derived:openfda.package_ndc |
| ndc11 | package | 53440000409 | derived:openfda.package_ndc |
| ndc11 | package | 53440000417 | derived:openfda.package_ndc |
| ndc11 | package | 53440000413 | derived:openfda.package_ndc |
| ndc11 | package | 53440000412 | derived:openfda.package_ndc |
| ndc11 | package | 53440000414 | derived:openfda.package_ndc |
| ndc11 | package | 53440000411 | derived:openfda.package_ndc |
| ndc11 | package | 53440000402 | derived:openfda.package_ndc |
| ndc11 | package | 53440000415 | derived:openfda.package_ndc |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.