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
- A-OX Welding Supply, LLC
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 7046ef16-a4f4-15b7-e053-2a91aa0a4f1a
- SPL ID
- 41d953d1-5988-866b-e063-6294a90a36ac
- Version
- 10
- Effective date
- 2025-10-23
- Source export date
- 2026-11-06
- 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/2026-11-06/b00a73f24c6ff050408c570063640e3d80d1f71dfc9a165d1cf072a25659445a/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 07:02:57
| 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 | 211781 | derived:openfda.application_number |
| application number | NDA211781 | openfda.application_number | |
| brand name | Helium | openfda.brand_name | |
| generic name | HELIUM | openfda.generic_name | |
| manufacturer name | A-OX Welding Supply, LLC | openfda.manufacturer_name | |
| ndc | package | 10297-006-02 | openfda.package_ndc |
| ndc | package | 10297-006-03 | openfda.package_ndc |
| ndc | package | 10297-006-01 | openfda.package_ndc |
| ndc | product | 10297-006 | openfda.product_ndc |
| ndc11 | package | 10297000603 | derived:openfda.package_ndc |
| ndc11 | package | 10297000602 | derived:openfda.package_ndc |
| ndc11 | package | 10297000601 | derived:openfda.package_ndc |
| rxcui | 310693 | openfda.rxcui | |
| spl id | 41d953d1-5988-866b-e063-6294a90a36ac | id | |
| spl set id | 7046ef16-a4f4-15b7-e053-2a91aa0a4f1a | set_id | |
| unii | 206GF3GB41 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.