FDA label 3515207a-f05e-002f-e063-6394a90aae2f

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
6e6866c2-e33c-3836-e053-2991aa0a8a40
SPL ID
3515207a-f05e-002f-e063-6394a90aae2f
Version
3
Effective date
2025-05-14
Source export date
2026-10-12
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:44:39

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

1. Discontinue use and ask a doctor if any adverse reactions occur such as rash, swelling or irritation after use or due to direct sunlight. 2. Do not use on damaged or broken skin. 3. Storage and Handling Precautions (A)Keep out of reach of children. (B)Keep out of direct sunlight. 4. Avoid contact with eyes. If there is any problem with this product, compensation is offered by based on ‘Consumer Dispute Resolution Criteria’, notice by The Fair Trade Commission. Customer Support Center +82-2-512-0478

Reported adverse events (FAERS/openFDA)#

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