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
- AGL Inhalation Therapy Co.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- b309a459-c8bc-4ac3-a4e2-3989a63be8a9
- SPL ID
- 4cc19ab7-134d-fce9-e063-6294a90ac0f5
- Version
- 16
- Effective date
- 2026-03-02
- Source export date
- 2026-10-12
- 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/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:13:25
| 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 | 205819 | derived:openfda.application_number |
| application number | NDA205819 | openfda.application_number | |
| brand name | Helium | openfda.brand_name | |
| generic name | HELIUM | openfda.generic_name | |
| manufacturer name | AGL Inhalation Therapy Co. | openfda.manufacturer_name | |
| ndc | package | 17575-005-03 | openfda.package_ndc |
| ndc | package | 17575-005-04 | openfda.package_ndc |
| ndc | package | 17575-005-06 | openfda.package_ndc |
| ndc | package | 17575-005-01 | openfda.package_ndc |
| ndc | package | 17575-005-02 | openfda.package_ndc |
| ndc | package | 17575-005-05 | openfda.package_ndc |
| ndc | product | 17575-005 | openfda.product_ndc |
| ndc11 | package | 17575000501 | derived:openfda.package_ndc |
| ndc11 | package | 17575000505 | derived:openfda.package_ndc |
| ndc11 | package | 17575000504 | derived:openfda.package_ndc |
| ndc11 | package | 17575000506 | derived:openfda.package_ndc |
| ndc11 | package | 17575000503 | derived:openfda.package_ndc |
| ndc11 | package | 17575000502 | derived:openfda.package_ndc |
| rxcui | 310693 | openfda.rxcui | |
| spl id | 4cc19ab7-134d-fce9-e063-6294a90ac0f5 | id | |
| spl set id | b309a459-c8bc-4ac3-a4e2-3989a63be8a9 | set_id | |
| unii | 206GF3GB41 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.