FDA label 6e75bbe4-117b-1aaa-e053-2a91aa0aadb0

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
4dc58253-4c87-495f-9b4b-ca76e7f54d01
SPL ID
6e75bbe4-117b-1aaa-e053-2a91aa0aadb0
Version
2
Effective date
2018-06-12
Source export date
2026-09-28
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:41:09

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 (For external use only) Do not use this product if Pregnant or breast-feeding or diabetes. Excessive dosage or short intervals between doses can result in high plasma levels and serious adverse effects, patients should be instructed to strictly adhere to the recommended dosage and administration guidelines set forth by a doctor. Some people may experience allergic reactions to ingredients in this product. Stop use and call a doctor for medical advice if mild irritation, redness, swelling, blurred vision, seizure, drowsiness, confusion, uneven heartbeats and any type of side effects or unusual symptoms.

Reported adverse events (FAERS/openFDA)#

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