Carbon Dioxide/Oxygen Mix
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/Oxygen Mix
- Generic name
- CARBON DIOXIDE/OXYGEN MIX
- Manufacturer
- NEXAIR, LLC
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 6b000266-aa36-4b0f-b4d1-f38e59d35c61
- SPL ID
- 4279406a-5209-1747-e063-6294a90a13d8
- Version
- 19
- Effective date
- 2025-10-31
- Source export date
- 2026-10-12
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:12:01
| 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 | 205849 | derived:openfda.application_number |
| application number | NDA205849 | openfda.application_number | |
| brand name | Carbon Dioxide/Oxygen Mix | openfda.brand_name | |
| generic name | CARBON DIOXIDE/OXYGEN MIX | openfda.generic_name | |
| manufacturer name | NEXAIR, LLC | openfda.manufacturer_name | |
| ndc | package | 12213-800-02 | openfda.package_ndc |
| ndc | package | 12213-800-03 | openfda.package_ndc |
| ndc | package | 12213-800-14 | openfda.package_ndc |
| ndc | package | 12213-800-01 | openfda.package_ndc |
| ndc | package | 12213-800-04 | openfda.package_ndc |
| ndc | package | 12213-800-06 | openfda.package_ndc |
| ndc | package | 12213-800-05 | openfda.package_ndc |
| ndc | package | 12213-800-58 | openfda.package_ndc |
| ndc | product | 12213-800 | openfda.product_ndc |
| ndc11 | package | 12213080002 | derived:openfda.package_ndc |
| ndc11 | package | 12213080014 | derived:openfda.package_ndc |
| ndc11 | package | 12213080058 | derived:openfda.package_ndc |
| ndc11 | package | 12213080004 | derived:openfda.package_ndc |
| ndc11 | package | 12213080005 | derived:openfda.package_ndc |
| ndc11 | package | 12213080003 | derived:openfda.package_ndc |
| ndc11 | package | 12213080006 | derived:openfda.package_ndc |
| ndc11 | package | 12213080001 | derived:openfda.package_ndc |
| spl id | 4279406a-5209-1747-e063-6294a90a13d8 | id | |
| spl set id | 6b000266-aa36-4b0f-b4d1-f38e59d35c61 | set_id | |
| unii | S88TT14065 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.