FDA label 2b0cb99e-f6cb-412d-9784-49fa5653ead8

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
027bfef9-f46c-4ddc-b65a-26f1b0b81a75
SPL ID
2b0cb99e-f6cb-412d-9784-49fa5653ead8
Version
2
Effective date
2023-12-21
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 01:37:47

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 have abdominal pain nausea fever vomiting with other medicines or if you are presently taking mineral oil if you are on a low salt diet longer than 7 days When using this product frequent or prolonged use may result in dependence on laxatives it may take up to 3 days for you to have a bowel movement Stop use and ask a doctor if rectal bleeding occurs symptoms persist, last for more than 7 days

Reported adverse events (FAERS/openFDA)#

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