FDA label 07ed0d89-9d76-4ed5-8d0e-6f002243966e

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
9ac7514b-fa72-46be-b932-ca69fe7ae07b
SPL ID
07ed0d89-9d76-4ed5-8d0e-6f002243966e
Version
3
Effective date
2019-12-13
Source export date
2026-11-06
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/d05434af5edc4383b7c7894a8f2d94df21171d17714450933cecdfc35cedfa3d/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 06:44:09

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 are currently taking mineral oil, unless directed by a doctor • when abdominal pain, nausea, or vomiting are present • for longer than one week unless directed by a doctor Ask a doctor before use if • you notice a sudden change in bowel habits that persists 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 If pregnant or breast-feeding ask a healthcare professional before use Keep out of reach of children In case of overdose, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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