FDA label 1f465097-395e-45f8-9a12-9fe50f598b0f

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
4c7d15eb-ace2-42e6-b03e-5702c50643ff
SPL ID
1f465097-395e-45f8-9a12-9fe50f598b0f
Version
1
Effective date
2016-08-12
Source export date
2026-09-28
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:16:55

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.