FDA label ac43188f-636f-4cb7-8277-30a892e27e0c

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
0caa2d3a-9fda-4dad-8bd2-2fca1a596b8b
SPL ID
ac43188f-636f-4cb7-8277-30a892e27e0c
Version
3
Effective date
2019-04-04
Source export date
2026-10-12
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 03:03:30

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. If you experience any of the following, please discontinue use and consult a dermatologist should irritation persist: 1) Sign of erythema, tumefaction, urtication, irritation 2) In case above symptoms arise when exposed to direct sunlight 2. Do not apply on the skin with wounds, eczema, or dermatitis. 3. Wash your eyes immediately if this product comes into contact with them. 4. Keep out of reach of babies and children.

Reported adverse events (FAERS/openFDA)#

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