FDA label f69f9485-2dc8-4fe9-b776-1f6e70677c19

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
ce060319-ca19-4d8c-b45a-d3d633efd73f
SPL ID
f69f9485-2dc8-4fe9-b776-1f6e70677c19
Version
5
Effective date
2022-11-04
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 05:45:30

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 laxative products for longer than 1 week unless directed by a doctor Ask a doctor before use if you have kidney disease a magnesium restricted diet a sodium restricted diet stomach pain, nausea or vomiting noticed a sudden change in bowel habits that lasts more than 1 week Ask a doctor or pharmacist before use if you are presently taking a prescription drug. When using this product do not exceed the maximum recommended daily dosage in a 24 hour period Stop use and ask a doctor if you have rectal bleeding or no bowel movement after use. These could be signs of a serious condition. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Reported adverse events (FAERS/openFDA)#

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