FDA label 9a008bb9-5625-fdd8-e053-2995a90a9d33

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
6bcb411a-f70f-058c-e053-2991aa0aa62a
SPL ID
9a008bb9-5625-fdd8-e053-2995a90a9d33
Version
2
Effective date
2019-12-18
Source export date
2026-10-12
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:34:25

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 when abdominal pain, nausea, or vomiting are present for more than one week unless directed by a doctor Ask a doctor before use if you are taking mineral oil have noticed a sudden change in bowel habits that lasts more than 2 weeks Stop use and ask a doctor if you have no bowel movement within 3 days you have rectal bleeding these could be signs of a serious condition a skin rash occurs you experience throat irritation

Reported adverse events (FAERS/openFDA)#

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