Helium
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
- Generic name
- HELIUM
- Manufacturer
- WSM SUPPLIER LLC.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 153317bb-7f55-0964-e063-6394a90a2922
- SPL ID
- 40a9f139-f16f-bb51-e063-6294a90a5536
- Version
- 3
- Effective date
- 2025-10-08
- Source export date
- 2026-11-06
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/4dafeb36642dffb72e2138939a956de402f722ea8c14c08cd87068efd3669f01/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 06:47:30
| 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 | 205843 | derived:openfda.application_number |
| application number | NDA205843 | openfda.application_number | |
| brand name | Helium | openfda.brand_name | |
| generic name | HELIUM | openfda.generic_name | |
| manufacturer name | WSM SUPPLIER LLC. | openfda.manufacturer_name | |
| ndc | package | 84120-001-06 | openfda.package_ndc |
| ndc | package | 84120-001-08 | openfda.package_ndc |
| ndc | package | 84120-001-03 | openfda.package_ndc |
| ndc | package | 84120-001-10 | openfda.package_ndc |
| ndc | package | 84120-001-04 | openfda.package_ndc |
| ndc | package | 84120-001-11 | openfda.package_ndc |
| ndc | package | 84120-001-09 | openfda.package_ndc |
| ndc | package | 84120-001-02 | openfda.package_ndc |
| ndc | package | 84120-001-07 | openfda.package_ndc |
| ndc | package | 84120-001-05 | openfda.package_ndc |
| ndc | package | 84120-001-01 | openfda.package_ndc |
| ndc | product | 84120-001 | openfda.product_ndc |
| ndc11 | package | 84120000108 | derived:openfda.package_ndc |
| ndc11 | package | 84120000109 | derived:openfda.package_ndc |
| ndc11 | package | 84120000107 | derived:openfda.package_ndc |
| ndc11 | package | 84120000111 | derived:openfda.package_ndc |
| ndc11 | package | 84120000102 | derived:openfda.package_ndc |
| ndc11 | package | 84120000106 | derived:openfda.package_ndc |
| ndc11 | package | 84120000104 | derived:openfda.package_ndc |
| ndc11 | package | 84120000103 | derived:openfda.package_ndc |
| ndc11 | package | 84120000105 | derived:openfda.package_ndc |
| ndc11 | package | 84120000101 | derived:openfda.package_ndc |
| ndc11 | package | 84120000110 | derived:openfda.package_ndc |
| rxcui | 997972 | openfda.rxcui | |
| spl id | 40a9f139-f16f-bb51-e063-6294a90a5536 | id | |
| spl set id | 153317bb-7f55-0964-e063-6394a90a2922 | set_id | |
| unii | 206GF3GB41 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.