FDA label 574d2e5f-ad2a-40eb-9d49-00007c005b9a

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
a0d9850a-8b86-470f-90df-3bce3eae742a
SPL ID
574d2e5f-ad2a-40eb-9d49-00007c005b9a
Version
4
Effective date
2021-12-16
Source export date
2026-09-28
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:31:14

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 abdominal pain, nausea or vomiting are present Ask a doctor before use if you notice a sudden change in bowel habits that persists over a period of 2 weeks you are presently taking mineral oil Stop use and ask a doctor if rectal bleeding or failure to have a bowel movement occur after use which may indicate a serious condition you need to use a laxative for more than 1 week 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.