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
2026-10-12
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/2026-10-12/7928c8e8c6256620071a8b7e5b93eb8dfa543649c08d17a01ea02251012ba58c/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:26:06

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.