Home FDA labels 3a115cf0-5500-b9e7-e063-6294a90a727f FDA label 3a115cf0-5500-b9e7-e063-6294a90a727f 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)
SPL set ID 8d0b341f-81b4-49a0-a712-1e0c79f778fc
SPL ID 3a115cf0-5500-b9e7-e063-6294a90a727f
Version 15
Effective date 2025-07-16
Source export date 2026-11-06
Source partition 8
Source file https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-11-06/db89d5ebfc3e02f44e8769334d799cd3436b05f779823ab00297f1f800c89ddf/drug-label-0008-of-0014.json.zip
Source manifest SHA-256 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run 20261108T063105Z
Imported at 2026-11-08 07:34:50 Harmonized identifier links# Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
Harmonized identifiers page 1 of 1 · 2 matching rows.
Warnings cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Warnings sections page 1 of 1 · 1 matching rows.
warnings Warnings Ask a doctor before use if you have •kidney disease •a magnesium-restricted diet •abdominal pain, nausea, or vomiting •noticed a sudden change in bowel habits that persists over a period of 2 weeks •already used a laxative for a period longer than 1 week
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.