Helium/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
- Helium/Oxygen Mix
- Generic name
- HELIUM/OXYGEN MIX
- Manufacturer
- NEXAIR, LLC
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 60dd4f4b-7132-385e-e053-2a91aa0ad5d6
- SPL ID
- 4279490a-a12b-05d4-e063-6394a90afa67
- Version
- 10
- Effective date
- 2025-10-31
- Source export date
- 2026-09-28
- Source partition
- 9
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:05:12
| 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 | Helium/Oxygen Mix | openfda.brand_name | |
| generic name | HELIUM/OXYGEN MIX | openfda.generic_name | |
| manufacturer name | NEXAIR, LLC | openfda.manufacturer_name | |
| ndc | package | 12213-801-12 | openfda.package_ndc |
| ndc | package | 12213-801-13 | openfda.package_ndc |
| ndc | package | 12213-801-02 | openfda.package_ndc |
| ndc | package | 12213-801-01 | openfda.package_ndc |
| ndc | package | 12213-801-03 | openfda.package_ndc |
| ndc | package | 12213-801-06 | openfda.package_ndc |
| ndc | package | 12213-801-28 | openfda.package_ndc |
| ndc | package | 12213-801-05 | openfda.package_ndc |
| ndc | package | 12213-801-04 | openfda.package_ndc |
| ndc | product | 12213-801 | openfda.product_ndc |
| ndc11 | package | 12213080103 | derived:openfda.package_ndc |
| ndc11 | package | 12213080101 | derived:openfda.package_ndc |
| ndc11 | package | 12213080105 | derived:openfda.package_ndc |
| ndc11 | package | 12213080112 | derived:openfda.package_ndc |
| ndc11 | package | 12213080102 | derived:openfda.package_ndc |
| ndc11 | package | 12213080104 | derived:openfda.package_ndc |
| ndc11 | package | 12213080106 | derived:openfda.package_ndc |
| ndc11 | package | 12213080113 | derived:openfda.package_ndc |
| ndc11 | package | 12213080128 | derived:openfda.package_ndc |
| rxcui | 413101 | openfda.rxcui | |
| spl id | 4279490a-a12b-05d4-e063-6394a90afa67 | id | |
| spl set id | 60dd4f4b-7132-385e-e053-2a91aa0ad5d6 | set_id | |
| unii | S88TT14065 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.