FDA label 2fc4d5d7-bf45-4b1d-893b-12d05f919527

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
dd15c7ac-091f-4a99-a0e6-473184148b61
SPL ID
2fc4d5d7-bf45-4b1d-893b-12d05f919527
Version
1
Effective date
2010-01-24
Source export date
2026-10-12
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:51:49

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

Warning: 1. Discontinue if the following symptom appears and consult with dermatologist for the continuous problem of use a) Discontinue use if redness, rash, irritation or tingling appears b) Discontinue if the above symptom appears by a direct sunlight on the applied part 2. Avoid the part for a cut, eczema or dermatitis

Reported adverse events (FAERS/openFDA)#

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