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
2026-11-06
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/2026-11-06/bbdc0a42bf44145a63c3752991067bece7e2a518be6cc14943d33c4987faa012/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:09:22

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.