Helium Oxygen Nitrogen 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 Nitrogen mixture
- Generic name
- HELIUM OXYGEN NITROGEN MIXTURE
- Manufacturer
- Linde Gas & Equipment Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 619c58a9-7eae-450a-aa89-0027a388ce06
- SPL ID
- d86bf9d1-3c4e-40fd-be55-fd59b28e902c
- Version
- 9
- Effective date
- 2025-12-30
- Source export date
- 2026-09-28
- Source partition
- 4
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:26:29
| 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 Nitrogen mixture | openfda.brand_name | |
| generic name | HELIUM OXYGEN NITROGEN MIXTURE | openfda.generic_name | |
| manufacturer name | Linde Gas & Equipment Inc. | openfda.manufacturer_name | |
| ndc | package | 59579-010-04 | openfda.package_ndc |
| ndc | package | 59579-010-01 | openfda.package_ndc |
| ndc | package | 59579-010-03 | openfda.package_ndc |
| ndc | package | 59579-010-06 | openfda.package_ndc |
| ndc | package | 59579-010-02 | openfda.package_ndc |
| ndc | package | 59579-010-05 | openfda.package_ndc |
| ndc | product | 59579-010 | openfda.product_ndc |
| ndc11 | package | 59579001005 | derived:openfda.package_ndc |
| ndc11 | package | 59579001004 | derived:openfda.package_ndc |
| ndc11 | package | 59579001002 | derived:openfda.package_ndc |
| ndc11 | package | 59579001006 | derived:openfda.package_ndc |
| ndc11 | package | 59579001003 | derived:openfda.package_ndc |
| ndc11 | package | 59579001001 | derived:openfda.package_ndc |
| rxcui | 1432283 | openfda.rxcui | |
| spl id | d86bf9d1-3c4e-40fd-be55-fd59b28e902c | id | |
| spl set id | 619c58a9-7eae-450a-aa89-0027a388ce06 | set_id | |
| unii | 206GF3GB41 | openfda.unii | |
| unii | N762921K75 | openfda.unii | |
| unii | S88TT14065 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.