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FDA label f5480c36-4401-49f2-b550-912e01527ac8

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
f5480c36-4401-49f2-b550-912e01527ac8
SPL ID
f5480c36-4401-49f2-b550-912e01527ac8
Version
1
Effective date
2011-09-07
Source export date
2026-10-12
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:42:45

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 -Do not use if you are currently 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 notice a sudden change in bowel habits that persists over a period of 2 weeks. Ask a doctor or pharmacist before use if You notice a sudden change in bowel habits that persists 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 Pregnancy/Breastfeeding Ask a health care 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.