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
2026-09-28
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/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:26:33
Harmonized routes table
Harmonized routes
RESPIRATORY (INHALATION)

Reported adverse events (FAERS/openFDA)#

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