FDA label 43f14f5e-aa40-44c9-9149-71776e64ea29

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
f7dfcfde-5dde-49bf-a22e-36be056407c2
SPL ID
43f14f5e-aa40-44c9-9149-71776e64ea29
Version
1
Effective date
2017-09-27
Source export date
2026-10-12
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:48:13

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: For external use only 1. If the following symptoms occur while using this product, discontinue use and consult your dermatologist: (1) Red spots, swelling, itching, or irritation (2) If the application area develops the symptoms above after exposure to direct sunlight 2. Do not apply on areas with injuries, eczema, or dermatitis. 3. Storage & Handling (1) Keep the cap closed after use. (2) Keep out of reach of children. (3) Keep away from direct sunlight and extreme high or low temperatures.

Reported adverse events (FAERS/openFDA)#

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