FDA label b1815933-6ddf-41c6-8859-eca043257f7e

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
d96986dd-eab8-4025-9987-77deb208972e
SPL ID
b1815933-6ddf-41c6-8859-eca043257f7e
Version
8
Effective date
2024-05-16
Source export date
2026-10-12
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/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:36:56

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 Drug I nteraction P recaution: D o not give this product to your child if your child is presently taking mineral oil , unless directed by a doctor. Ask a doctor before using any laxative if your child has a sudden change in bowel habits lasting more than 2 weeks already used a laxative for more than 1 week If constipation continues after 1 week of use, contact your child's doctor Stop using this product and consult a doctor if your child has rectal bleeding no bowel movement within 72 hours of using this product These symptoms may be signs of a serious condition. Keep out of reach of children In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Reported adverse events (FAERS/openFDA)#

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