FDA.reportPublic FDA data

FDA label ffe6ec92-ecd2-44de-8958-a17ea63d2cc0

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
80c93fd4-d764-4e95-a914-547b9675e868
SPL ID
ffe6ec92-ecd2-44de-8958-a17ea63d2cc0
Version
2
Effective date
2013-01-30
Source export date
2026-09-28
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/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:16:15

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. If pregnant or breast-feeding, ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

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