FDA label 5bd25827-7ddd-40e8-a6a5-80dafd40c452

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
42273ecf-6245-4fb3-87d4-d41d509b10d8
SPL ID
5bd25827-7ddd-40e8-a6a5-80dafd40c452
Version
3
Effective date
2020-10-20
Source export date
2026-10-12
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:33:40

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: ​ ​ ​This product is you are presently taking mineral oil, unless directed by a doctor. Laxative products for longer than 1 week, unless directed by a doctor Ask a doctor before use if you have: Stomach pain, nausea, vomiting, a sudden change in bowel movements that persists over 2 weeks Stop use and ask a doctor if you have: Rectal bleeding or fail to have a bowel movement after use of a laxative. These could be signs of a serious condition.

Reported adverse events (FAERS/openFDA)#

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