Aurum iodatum

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
Aurum iodatum
Generic name
GOLD MONOIODIDE
Manufacturer
Boiron
Product type
HUMAN OTC DRUG
SPL set ID
6c40ea02-4076-3880-e053-2991aa0ad6c1
SPL ID
3bf73fbe-fa38-c3d8-e063-6294a90aef07
Version
4
Effective date
2025-08-09
Source export date
2026-10-27
Source partition
9
Source file
https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-27/a73bb3b6a943796a18cd4bcd0917240b579be4636d00e6e39481bafbd8093f69/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run
20261027T193451Z
Imported at
2026-10-27 20:36:14
Harmonized routes table
Harmonized routes
ORAL

Reported adverse events (FAERS/openFDA)#

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