Home FDA labels 23e46dbd-61b3-0bd1-e054-00144ff88e88 FDA label 23e46dbd-61b3-0bd1-e054-00144ff88e88 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 23e46dbd-61b2-0bd1-e054-00144ff88e88
SPL ID 23e46dbd-61b3-0bd1-e054-00144ff88e88
Version 1
Effective date 2015-10-28
Source export date 2026-11-06
Source partition 7
Source file https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-11-06/824fe785252d7061429a95ddb6de517ee399ef628d34e8fdcc3591ded286ae33/drug-label-0007-of-0014.json.zip
Source manifest SHA-256 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run 20261108T063105Z
Imported at 2026-11-08 07:28:13 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 Warnings For External use only. WHEN USING THIS PRODUCT Avoid contact with eyes. Avoid unnecessary sun exposure and use a sunscreen to prevent darkening from reoccuring. Test overnight on Inside of elbow before use. If skin irritation occurs, discontinue use and consult a doctor.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.