FDA label c6798bd1-561a-4634-8b38-5e8b9b6a402a

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
af84c8aa-02fa-758f-0072-2eedf60e68ae
SPL ID
c6798bd1-561a-4634-8b38-5e8b9b6a402a
Version
3
Effective date
2025-04-03
Source export date
2026-11-06
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/39f3c0903357a80632a5484c9d6a804272f4b297080aa9c5a01a84db133f7a03/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 08:00:43

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 For rectal use only Do not use laxative products for a period longer than one week unless directed by a doctor Ask a doctor before use if you have • abdominal pain, nausea or vomiting • a sudden change in bowel habits that lasts longer than 2 weeks Stop use and ask a doctor if rectal bleeding occurs or you fail to have a bowel movement after using a laxative. This may indicate a serious condition.

Reported adverse events (FAERS/openFDA)#

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