Heliox

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 (canonical bytes are SHA-256 checked before publication)

Brand name
Heliox
Generic name
HELIOX
Manufacturer
A-OX Welding Supply, LLC
Product type
HUMAN PRESCRIPTION DRUG
SPL set ID
eadb2cba-9080-77e8-e053-2a95a90afe03
SPL ID
41d955de-b739-1d45-e063-6394a90a1bc5
Version
4
Effective date
2025-10-23
Source export date
2026-10-30
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-30/a3e33fe073aa0aa94eb690c6684c74434c63cebfbf7c5530205a2c3e957ecb8b/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run
20261102T182004Z
Imported at
2026-11-02 19:41:10
Harmonized routes table
Harmonized routes
RESPIRATORY (INHALATION)

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.