FDA label 7c47361f-0d18-5d41-e053-2a91aa0aea14

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
53e8fc4a-ffe7-48bc-afcf-5310240ac343
SPL ID
7c47361f-0d18-5d41-e053-2a91aa0aea14
Version
6
Effective date
2018-12-05
Source export date
2026-09-28
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:30:20

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 Allergy alert may cause allergic reaction in people sensitive to inhaled or ingested psyllium Choking taking this product without adequate fluid may cause it to swell and block your throat or esophagus and may cause choking Do not take this product if you have difficulty in swallowing if you experience chest pain, vomiting or difficulty in swallowing or breathing after taking this product, seek immediate medical attention Ask a doctor before use if you have abdominal pain, nausea, vomiting or rectal bleeding a sudden change in bowel habits that persist over a period of 2 weeks constipation associated with gastrointestinal disorders Ask a doctor or pharmacist before use if you are taking any other drug take this product 2 or more hours before or after other drugs all laxatives may affect how other drugs work Stop use and ask a doctor if constipation persists beyond 7 days. This could be a sign condition Keep out of reach of children In case of overdose, get 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.