FDA.reportPublic FDA data

FDA label 727b02f3-bcd1-4568-9a0d-7723b6264800

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
727b02f3-bcd1-4568-9a0d-7723b6264800
SPL ID
727b02f3-bcd1-4568-9a0d-7723b6264800
Version
1
Effective date
2010-07-30
Source export date
2026-10-12
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:29:19

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 this product if you are presently taking mineral oil, unless directed by a doctor laxative products for more than 1 week unless directed by a doctor Ask a doctor before use if you have stomach pain nausea vomiting a sudden change in bowel habits that persists over 2 weeks Stop use and ask a doctor if you have have rectal bleeding fail to have a bowel movement after the use of a laxative 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 right away.

Reported adverse events (FAERS/openFDA)#

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