FDA label 893191c3-950c-4239-acb0-09e97a2357da

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
dccb0b89-87d9-4a27-8b3b-39e8c84e3a3e
SPL ID
893191c3-950c-4239-acb0-09e97a2357da
Version
2
Effective date
2017-03-31
Source export date
2026-10-12
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:35:56

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 using if you have stomach pain nausea vomiting noticed a sudden change in bowel movements that continues over a period of 2 weeks Stop use and ask a doctor if you have rectal bleeding you fail to have a bowel movement after use These may indicate a serious condition. If pregnant or breast-feeding If pregnant or breast-feeding, ask a health care professional before use. Keep out of reach of children Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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