FDA label 6ec813e4-5909-414d-ab9d-54c79b102d76

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: 96a3a9f4-a6c4-4055-a0c1-79c6267a42d0
SPL ID: 6ec813e4-5909-414d-ab9d-54c79b102d76
Version: 5
Effective date: 2021-04-27
Source export date: 2026-10-12
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:51:00

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 2 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
spl id		6ec813e4-5909-414d-ab9d-54c79b102d76	id
spl set id		96a3a9f4-a6c4-4055-a0c1-79c6267a42d0	set_id

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 1 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 breastfeeding ask a health care 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.