FDA label d56df985-98e1-4304-a9a5-0acc78075a20

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
b0509951-a720-4d4d-85df-1ad1993c05c1
SPL ID
d56df985-98e1-4304-a9a5-0acc78075a20
Version
3
Effective date
2025-05-29
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 01:40:33

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 • laxative products for longer than 1 week unless directed by a doctor • If you are now taking mineral oil, unless directed by a doctor Ask a doctor before use if you have • stomach pain, nausea, vomiting • 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 of a laxative. These may indicate a serious condition 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 immediately.

Reported adverse events (FAERS/openFDA)#

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