Home FDA labels 7c3da1dd-8ad0-422b-882b-2591ea6c00ff FDA label 7c3da1dd-8ad0-422b-882b-2591ea6c00ff 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 d03befe9-4f75-4395-995d-245843e35370
SPL ID 7c3da1dd-8ad0-422b-882b-2591ea6c00ff
Version 1
Effective date 2013-04-30
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 01:42:05 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 on hands. Avoid contact with eyes. In case of contact, flush thoroughly with water. Do not inhale or ingest. Avoid contact with broken skin. Discontinue use if irritation or redness develops. If condition persists for more than 72 hours, consult a doctor.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.