FDA label 96159869-6045-5391-e053-2a95a90ae1b1

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
5a7980c2-8f86-21cb-e053-2a91aa0ada8d
SPL ID
96159869-6045-5391-e053-2a95a90ae1b1
Version
2
Effective date
2019-10-29
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 01:42:12

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

Cautions : 1. When you use this product and find any of following problems, stop using it. if you keep using it despite the problem, the symptom will get worse, so you will have to go see a dermatologist. - During use, if you have red spots, swelling, itching, or any other stimuli. - if the applied region has any problem above for direct light. 2. Do not use the product on wound or dermatitis. 3.Attentive points for storage and treatment : - Store it in the place where infants or children cannot touch - do not store it where it has either high or low temperature or there is direct light.

Reported adverse events (FAERS/openFDA)#

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