Helium Oxygen mixture
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
- Helium Oxygen mixture
- Generic name
- HELIUM OXYGEN MIXTURE
- Manufacturer
- Linde Gas & Equipment Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- ef29f856-4675-4bb7-adef-67d7c6f27439
- SPL ID
- e4730863-853f-4f34-b148-1c03ca465317
- Version
- 9
- Effective date
- 2025-01-24
- Source export date
- 2026-10-22
- 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/2026-10-22/0bafccaf0213baa649cda9c1c2365d28432e10cf46f4167b2ea41290b5cac2b8/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- 5de9d3c3492926d1703b492ae4d29b036ac5be73edfcb92a6cd5eb95a2acef9c
- Import run
- 20261023T001338Z
- Imported at
- 2026-10-23 01:05:54
| 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 |
|---|---|---|---|
| brand name | Helium Oxygen mixture | openfda.brand_name | |
| generic name | HELIUM OXYGEN MIXTURE | openfda.generic_name | |
| manufacturer name | Linde Gas & Equipment Inc. | openfda.manufacturer_name | |
| ndc | package | 59579-009-10 | openfda.package_ndc |
| ndc | package | 59579-009-07 | openfda.package_ndc |
| ndc | package | 59579-009-06 | openfda.package_ndc |
| ndc | package | 59579-009-09 | openfda.package_ndc |
| ndc | package | 59579-009-03 | openfda.package_ndc |
| ndc | package | 59579-009-05 | openfda.package_ndc |
| ndc | package | 59579-009-02 | openfda.package_ndc |
| ndc | package | 59579-009-11 | openfda.package_ndc |
| ndc | package | 59579-009-01 | openfda.package_ndc |
| ndc | package | 59579-009-08 | openfda.package_ndc |
| ndc | package | 59579-009-04 | openfda.package_ndc |
| ndc | product | 59579-009 | openfda.product_ndc |
| ndc11 | package | 59579000906 | derived:openfda.package_ndc |
| ndc11 | package | 59579000911 | derived:openfda.package_ndc |
| ndc11 | package | 59579000901 | derived:openfda.package_ndc |
| ndc11 | package | 59579000910 | derived:openfda.package_ndc |
| ndc11 | package | 59579000902 | derived:openfda.package_ndc |
| ndc11 | package | 59579000908 | derived:openfda.package_ndc |
| ndc11 | package | 59579000903 | derived:openfda.package_ndc |
| ndc11 | package | 59579000909 | derived:openfda.package_ndc |
| ndc11 | package | 59579000905 | derived:openfda.package_ndc |
| ndc11 | package | 59579000904 | derived:openfda.package_ndc |
| ndc11 | package | 59579000907 | derived:openfda.package_ndc |
| rxcui | 542169 | openfda.rxcui | |
| spl id | e4730863-853f-4f34-b148-1c03ca465317 | id | |
| spl set id | ef29f856-4675-4bb7-adef-67d7c6f27439 | set_id | |
| unii | 206GF3GB41 | openfda.unii | |
| unii | S88TT14065 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.