FDA label 5d23093e-30d7-488d-8df2-0ec78055321b

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: 299ac7ea-3335-4d9d-893d-1ace0984b03e
SPL ID: 5d23093e-30d7-488d-8df2-0ec78055321b
Version: 7
Effective date: 2016-03-09
Source export date: 2026-09-28
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:22:36

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		5d23093e-30d7-488d-8df2-0ec78055321b	id
spl set id		299ac7ea-3335-4d9d-893d-1ace0984b03e	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 presently 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 continues 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 health 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.