Home FDA labels b72803d6-b402-2614-e053-2a95a90affe3 FDA label b72803d6-b402-2614-e053-2a95a90affe3 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 9511a3ad-8d63-5f7d-e053-2995a90aa0f6
SPL ID b72803d6-b402-2614-e053-2a95a90affe3
Version 2
Effective date 2020-12-23
Source export date 2026-09-28
Source partition 1
Source file https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:13:21 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 Only use as directed Do not allow contact with eyes Do not bandage or apply local heat such as heating pads to the area of use STOP use and ask a doctor if: symptoms last more than 7 days or clear up and occur again within a few days condition worsens
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.