FDA label c37cd40d-1be8-4230-8102-744c7c1a20e2

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
d43ab97f-6b82-44cb-a1d6-975510b4de65
SPL ID
c37cd40d-1be8-4230-8102-744c7c1a20e2
Version
1
Effective date
2019-04-19
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 01:48:08

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 Warnings: 1. Consult a physician if red spots, swollenness, itchiness, or any other adnormal symptoms or side effects develops on the applied area during or after use or under direct sunlight. 2. Do not use on wound, etc. 3. Precautions for handling and storage a) Keep out of the reach of children b) Avoid direct sunlight

Reported adverse events (FAERS/openFDA)#

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