FDA label 037d924d-f832-472b-8a57-5af4eb529822

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
36eba7c7-de86-4b35-863f-c4ae0bbf2e0c
SPL ID
037d924d-f832-472b-8a57-5af4eb529822
Version
1
Effective date
2021-09-24
Source export date
2026-10-22
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/2026-10-22/6983e0043e02b7c5b54ab7cac56ed79eae60cfdeef16cfdd964bf5591555d29c/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
5de9d3c3492926d1703b492ae4d29b036ac5be73edfcb92a6cd5eb95a2acef9c
Import run
20261023T001338Z
Imported at
2026-10-23 00:23:50

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 1. Stop using and see a doctor in case of having following symptoms while using this product. ⓐ Red spots, swelling, itching, etc. While using. ⓑ In case of having the same symptoms due to direct sunlight. 2. Do not use on the part where you have a scar, eczema, or dermatitis. 3. Cautions for treatment and keeping. ⓐ Keep it out of children’s reach. ⓑ Avoid direct sunlight. ⓒ For external use only.

Reported adverse events (FAERS/openFDA)#

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