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
- 2026-10-12
- 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/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:38:30
| 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 | 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.