FDA label 071dd31b-6aee-4981-e063-6294a90ada5c

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
50314e6b-c2bf-4e6e-94e8-220044c959d9
SPL ID
071dd31b-6aee-4981-e063-6294a90ada5c
Version
4
Effective date
2023-10-07
Source export date
2026-09-28
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/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:52:34

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 Do not use laxative products for longer than 1 week unless directed by a doctor. Ask a doctor before use if you have Kidney disease A sodium restricted diet Noticed a sudden change in bowel habits that lasts more than 1 week A magnesium restricted diet Stomach pain, nausea or vomiting Ask a doctor or pharmacist before use if you are presently taking a prescription drug. When using this product, do not exceed the maximum recommended daily dosage in a 24 hour period. Stop use and ask a doctor if you have rectal bleeding or no bowel movement after use. These could be signs of a serious condition. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Reported adverse events (FAERS/openFDA)#

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