FDA label 59828743-fd4a-4633-a726-5c5fc820dd13

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
a0715881-66db-4203-80ae-823013ac3fcf
SPL ID
59828743-fd4a-4633-a726-5c5fc820dd13
Version
4
Effective date
2020-05-26
Source export date
2026-10-12
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:36:25

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 When using this product use only as directed avoid getting into the eyes and mucous membranes do not bandage tightly or use with a heating pad do not apply to wounds or damaged skin Stop use and ask doctor if condition worsens symptoms persist for more than 7 days or clear up and occur again within a few days excessive skin irritation or redness occurs If pregnant or breast-feeding, ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.