FDA label a119e1f3-6376-4827-917f-cd57cbeb0f46

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
e6cf8b0f-adde-4679-8ac3-efed74b07348
SPL ID
a119e1f3-6376-4827-917f-cd57cbeb0f46
Version
3
Effective date
2020-06-24
Source export date
2026-10-12
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/7928c8e8c6256620071a8b7e5b93eb8dfa543649c08d17a01ea02251012ba58c/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:25:51

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: In case of abnormal symptom or side effect such as red spot, swelling or itching by direct sunlight, consult with a specialist 2) Avoid applying on injured skin 3) Storage precautions a) keep away from children b) keep away from direct sunlight 4) avoid eye area while using. Others. Be careful if you're highly sensitive to attach bandages or to blisters. If there is something wrong with this product, customer will be compensated according to the Fair Trade Commission's Notice of Consumer Dispute Resolution.

Reported adverse events (FAERS/openFDA)#

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