FDA label 21da3eaa-aa33-40e9-8b91-9ce19783996c

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: 87a3e05e-d02f-40d7-af82-eb50bf669b96
SPL ID: 21da3eaa-aa33-40e9-8b91-9ce19783996c
Version: 3
Effective date: 2024-10-11
Source export date: 2026-10-12
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:31:10

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 2 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
spl id		21da3eaa-aa33-40e9-8b91-9ce19783996c	id
spl set id		87a3e05e-d02f-40d7-af82-eb50bf669b96	set_id

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 Using more than one enema in 24 hours can be harmful. Ask a doctor before using this product if you are on a sodium-restricted diet have kidney disease are pregnant or nursing a baby Ask a doctor before using any laxative if you: have abdominal pain, nausea, or vomiting have a sudden change in bowel habits lasting more than 2 weeks have already used a laxative for more than 1 week Stop using this product and consult a doctor if you have rectal bleeding have no bowel movement after the enema is given These symptoms may indicate a serious condition.

Reported adverse events (FAERS/openFDA)#

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