FDA.reportPublic FDA data

FDA label 6327f079-17cc-ecb1-e053-2a91aa0a4f7e

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
6327f079-17cb-ecb1-e053-2a91aa0a4f7e
SPL ID
6327f079-17cc-ecb1-e053-2a91aa0a4f7e
Version
1
Effective date
2018-01-19
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 05:29:53

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

DO NOT USE IF -you have a medical condition or caffeine sensitive Ask doctor of pharmacist before use if you have - heart disease or an irregular hearbeat; high blood pressure; stomach ulcers; diabetes; allergies to other medications STOP USE AND SPEAK TO A DOCTOR IF - any of the following occur - mouth, teeth or jaw problems, irregular heartbeat or palpitations, you develop symptoms of an allergic reaction - such as difficulty breathing or a rash. IF PREGNANT OR BREAST FEEDING - ask a health professional before use

Reported adverse events (FAERS/openFDA)#

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