FDA label 29bb0975-f9df-8753-e063-6394a90a2be2

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
4bb375a0-8ec3-4769-9802-832b8a280e7d
SPL ID
29bb0975-f9df-8753-e063-6394a90a2be2
Version
5
Effective date
2024-12-20
Source export date
2026-11-06
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/2026-11-06/824fe785252d7061429a95ddb6de517ee399ef628d34e8fdcc3591ded286ae33/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:24:15

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 if you cannot swallow without chewing Ask a doctor before use if you have ■ stomach pain, nausea or vomiting ■ a sudden change in bowel habits that lasts more than 2 weeks When using this product ■ do not chew or crush tablet(s) ■ it may cause stomach discomfort, faintness and cramps ■ do not use within 1 hour after taking an antacid or milk

Reported adverse events (FAERS/openFDA)#

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