FDA label 2df9d7f8-87a2-4f2c-bd28-a4e1f9153cc0

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
21591790-07ec-7a28-5cdf-bd734d91d58b
SPL ID
2df9d7f8-87a2-4f2c-bd28-a4e1f9153cc0
Version
3
Effective date
2024-02-16
Source export date
2026-09-28
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:34:58

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: Advertencia: Abdominal cramps, nausea, vomiting, diarrhea, headache, or dizziness sometimes occur after taking this drug. If any of these conditions persist consult a doctor. If you are pregnant or have liver disease, do not take this product unless directed by a doctor. Retortijones, nausea, vomito, diarrea, dolor de cabeza o mareo ocasionalmente puede ocurrir después de tomar este producto. Consulté a un medico si persiste alguno de estos síntomas. Si esta embarazada o tiene enfermedad de hígado no use si no dirigido por su doctor

Reported adverse events (FAERS/openFDA)#

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