FDA label 6a617c11-4c53-459f-ad31-bad2c73c1828

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: e4877c84-4609-4022-b3af-39eca8fa8f19
SPL ID: 6a617c11-4c53-459f-ad31-bad2c73c1828
Version: 6
Effective date: 2012-05-15
Source export date: 2026-10-12
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:29:40

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		6a617c11-4c53-459f-ad31-bad2c73c1828	id
spl set id		e4877c84-4609-4022-b3af-39eca8fa8f19	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

Do not use Laxative products for longer than 1 week, unless directed by a doctor Ask a doctor before using if you have: Stomach pain, nausea, vomiting, or noticed a sudden change in bowel movements that continues over a period of 2 weeks Stop use ans ask a doctor if you have rectal bleeding or you fail to have a bowel movement after use. These may indicate a serious condition. If pregnant or breast-feeding , 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.