FDA label 3b2a6a3b-0ca3-41fc-a1b3-c95d6105b042

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: d159c229-318c-445b-87fb-ef0797903d35
SPL ID: 3b2a6a3b-0ca3-41fc-a1b3-c95d6105b042
Version: 9
Effective date: 2022-11-22
Source export date: 2026-10-12
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:08:37

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		3b2a6a3b-0ca3-41fc-a1b3-c95d6105b042	id
spl set id		d159c229-318c-445b-87fb-ef0797903d35	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 have noticed 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 you are pregnant or breast-feeding, ask a health professional before use. This unit dose package is not child resistant and is Intended for Institutional Use Only.

Reported adverse events (FAERS/openFDA)#

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