FDA label 46e1796a-dc76-4377-9eed-2c48aed8567e

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
91891b34-b18e-4979-bbaf-e664e9a01150
SPL ID
46e1796a-dc76-4377-9eed-2c48aed8567e
Version
1
Effective date
2010-02-24
Source export date
2026-09-28
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:33:05

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 abdominal discomfort, faintness, rectal burning, and mild cramps. 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 torn, damaged, or open 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 serious 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.