FDA label 5d77ae33-8fe6-41f1-b028-ba5a6d003b03

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
5dcea9dc-51f7-4de8-ba41-1bebfd2a6671
SPL ID
5d77ae33-8fe6-41f1-b028-ba5a6d003b03
Version
1
Effective date
2009-12-07
Source export date
2026-09-28
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:50:33

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 For rectal use only. May cause rectal discomfort or a burning sensation. Do not use more than one per day for a period of longer than one week unless directed by a doctor laxative products when abdominal pain, nausea, or vomiting are present unless directed by a doctor if seal under product lid is damaged, missing or broken. Ask a doctor before use if you have noticed a sudden change in bowel habits that persist over a period of two weeks if you are pregnant or nursing a baby Stop use and ask a doctor if you have rectal bleeding or fail to have a bowel movement after using a laxative. This may indicate a condition. Keep out of reach of children If swallowed, 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.