FDA label 2bc0590a-7e90-a82b-e063-6294a90a89c1

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
c1d58e0c-a66d-48d0-b1c3-cb0546595b42
SPL ID
2bc0590a-7e90-a82b-e063-6294a90a89c1
Version
4
Effective date
2025-01-15
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 06:36:58

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

CAUTIONS AND WARNINGS Keep out of the reach of children. If overdose or accidental ingestion occurs, call a Poison Control Center immediately. Discontinue use and consult a health care practitioner if symptoms persist and/or worsen after 7 days or re-occur within a few days. Consult a healthcare practitioner prior to use if you are pregnant or breastfeeding . Consult a healthcare practitioner prior to use if you are taking anticoagulant medications. Store protected from direct light and moisture at room temperature.

Reported adverse events (FAERS/openFDA)#

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