FDA label 5d23093e-30d7-488d-8df2-0ec78055321b

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
299ac7ea-3335-4d9d-893d-1ace0984b03e
SPL ID
5d23093e-30d7-488d-8df2-0ec78055321b
Version
7
Effective date
2016-03-09
Source export date
2026-11-06
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/2026-11-06/b00a73f24c6ff050408c570063640e3d80d1f71dfc9a165d1cf072a25659445a/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 06:58:39

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 ■ if you are presently taking mineral oil, unless directed by a doctor ■ when abdominal pain, nausea, or vomiting are present ■ for longer than 1 week, unless directed by a doctor Ask a doctor before use if you have noticed a sudden change in bowel habits 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 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.