Oxygen Helium Mixture 20/80
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
- Oxygen Helium Mixture 20/80
- Generic name
- OXYGEN HELIUM MIXTURE 20/80
- Manufacturer
- AGL Inhalation Therapy Co.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- e5f7f27b-5c9d-47f3-8312-641cb8b3ffd1
- SPL ID
- 41c377c4-ee36-0c64-e063-6394a90a6cb7
- Version
- 14
- Effective date
- 2026-01-01
- Source export date
- 2026-09-28
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:17:23
| 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 | 205767 | derived:openfda.application_number |
| application number | NDA205767 | openfda.application_number | |
| brand name | Oxygen Helium Mixture 20/80 | openfda.brand_name | |
| generic name | OXYGEN HELIUM MIXTURE 20/80 | openfda.generic_name | |
| manufacturer name | AGL Inhalation Therapy Co. | openfda.manufacturer_name | |
| ndc | package | 17575-192-03 | openfda.package_ndc |
| ndc | package | 17575-192-02 | openfda.package_ndc |
| ndc | package | 17575-192-01 | openfda.package_ndc |
| ndc | product | 17575-192 | openfda.product_ndc |
| ndc11 | package | 17575019201 | derived:openfda.package_ndc |
| ndc11 | package | 17575019203 | derived:openfda.package_ndc |
| ndc11 | package | 17575019202 | derived:openfda.package_ndc |
| rxcui | 413101 | openfda.rxcui | |
| spl id | 41c377c4-ee36-0c64-e063-6394a90a6cb7 | id | |
| spl set id | e5f7f27b-5c9d-47f3-8312-641cb8b3ffd1 | set_id | |
| unii | S88TT14065 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.