Home FDA labels 9115b517-7163-4b7a-b471-94890e82ec4c FDA label 9115b517-7163-4b7a-b471-94890e82ec4c 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 a12761e4-46c0-4eea-b5f3-ceccaea7efa3
SPL ID 9115b517-7163-4b7a-b471-94890e82ec4c
Version 8
Effective date 2012-08-13
Source export date 2026-11-06
Source partition 2
Source file https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-11-06/4dafeb36642dffb72e2138939a956de402f722ea8c14c08cd87068efd3669f01/drug-label-0002-of-0014.json.zip
Source manifest SHA-256 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run 20261108T063105Z
Imported at 2026-11-08 06:53:19 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 For External use only. When using this product do not get into eyes. If pregnant or breastfeeding, ask a professional before use. Stop use and ask doctor if conditions worsen, symptoms last more than 7days or clear up and occur again in a few days.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.