FDA label 573d47b3-4169-4f92-8561-5078743acdd4

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
714528d0-2813-4423-8a2d-601a6aabda96
SPL ID
573d47b3-4169-4f92-8561-5078743acdd4
Version
1
Effective date
2016-08-12
Source export date
2026-10-12
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:34:40

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: - If the following side effects occur, immediately discontinue use. Before resuming use, consult a dermatologist as continual use may worsen symptoms. ①If red spots swelling, itching, irritation, or other discomforts occur after using the product. ②If the above symptoms occur on the applied area after exposure to direct sunlight. - Do not use on open wounds or on areas of skin exhibiting signs of eczema or dermatitis. - Storage and handling precautions. ①Keep product out of reach of infants and children. ②Do not store in places subject to high or cold temperatures or under exposure to direct sunlight. ③Use care to avoid eye contact when using this product.

Reported adverse events (FAERS/openFDA)#

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