Home FDA labels 6669d03d-1735-edc5-e053-2991aa0acb24 FDA label 6669d03d-1735-edc5-e053-2991aa0acb24 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 96632796-3cd3-4294-97e4-cd3fec7f429e
SPL ID 6669d03d-1735-edc5-e053-2991aa0acb24
Version 2
Effective date 2018-03-02
Source export date 2026-09-28
Source partition 3
Source file https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:21:41 Harmonized identifier links# Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
Harmonized identifiers page 1 of 1 · 2 matching rows.
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 - Stop using if sensitivities occurs and consult with dermatologist - sensitivities such as red marks, intumescence, urtication, irritation during use -Have sensitivities as above on applied part by direct sun ray - Do not store at high and low temperatures and avoid sunlight.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.