Home FDA labels 807982a5-c00f-476e-a20e-3315826756ba FDA label 807982a5-c00f-476e-a20e-3315826756ba 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 54d7250e-6aaa-4fc8-88b3-2fee58ebaf73
SPL ID 807982a5-c00f-476e-a20e-3315826756ba
Version 1
Effective date 2011-10-18
Source export date 2026-10-12
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/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 01:42:43 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 - Do not use over deep or puncture wounds, infections, or lacerations. For external use only. - When using this product do not get into eyes. If contact occurs, rinse eyes throughout with water. - Stop use and ask a doctor if condition worsens or does not improve with 7 days.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.