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
- Roberts Oxygen Company, Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 554faa48-7fc2-4d1a-b223-82cf107b144f
- SPL ID
- 43cecff0-1ded-dece-e063-6394a90a8c6e
- Version
- 7
- Effective date
- 2025-11-17
- Source export date
- 2026-11-06
- 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/2026-11-06/2233cb6af8c6b55a5e4a05449e8db0d2f259f3c061d5d001b654a8bea1cc1db2/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 07:52:44
| 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 | 213609 | derived:openfda.application_number |
| application number | NDA213609 | openfda.application_number | |
| brand name | Helium | openfda.brand_name | |
| generic name | HELIUM | openfda.generic_name | |
| manufacturer name | Roberts Oxygen Company, Inc. | openfda.manufacturer_name | |
| ndc | package | 46123-800-06 | openfda.package_ndc |
| ndc | package | 46123-800-04 | openfda.package_ndc |
| ndc | package | 46123-800-07 | openfda.package_ndc |
| ndc | package | 46123-800-02 | openfda.package_ndc |
| ndc | package | 46123-800-01 | openfda.package_ndc |
| ndc | package | 46123-800-03 | openfda.package_ndc |
| ndc | package | 46123-800-05 | openfda.package_ndc |
| ndc | product | 46123-800 | openfda.product_ndc |
| ndc11 | package | 46123080003 | derived:openfda.package_ndc |
| ndc11 | package | 46123080005 | derived:openfda.package_ndc |
| ndc11 | package | 46123080001 | derived:openfda.package_ndc |
| ndc11 | package | 46123080006 | derived:openfda.package_ndc |
| ndc11 | package | 46123080007 | derived:openfda.package_ndc |
| ndc11 | package | 46123080004 | derived:openfda.package_ndc |
| ndc11 | package | 46123080002 | derived:openfda.package_ndc |
| rxcui | 310693 | openfda.rxcui | |
| spl id | 43cecff0-1ded-dece-e063-6394a90a8c6e | id | |
| spl set id | 554faa48-7fc2-4d1a-b223-82cf107b144f | set_id | |
| unii | 206GF3GB41 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.