FDA label f0aa7245-b91f-499c-b009-77b00e41c9c8

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
ae9a1c12-8662-4f5d-8435-e51dc2b45780
SPL ID
f0aa7245-b91f-499c-b009-77b00e41c9c8
Version
2
Effective date
2018-01-17
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 02:33:10

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 This product does not contain a child resistant cap. Keep out of reach of children. In case of accidental overdose, contact a doctor or a poison control center. Cautions Stop use if you are having rectal bleeding or failure to have a bowel movement after use. If adverse effects call 1-800-736- 3437 Unless directed by your doctor Do not take any laxative if you are having abdominal pain, nausea, or vomiting. Laxative products should not be used longer than a week. Ask a pharmacist or doctor if • You have noticed a sudden change in bowel habits that persist over two weeks after using this product. • You are pregnant or breast feeding before use.

Reported adverse events (FAERS/openFDA)#

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