FDA label e91a2ee4-b089-403b-8978-ae02bc2204f8

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
13f1af21-03d3-45ac-b4bc-9c68b12d1695
SPL ID
e91a2ee4-b089-403b-8978-ae02bc2204f8
Version
3
Effective date
2021-06-01
Source export date
2026-09-28
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/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:12:34

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 Cautions: 1. Stop using a product if you have any unusual symptoms mentioned below. Contacting with a dermatologist is recommended rather than using it continuously and making the symptom worse. 1) Red spots, swellings, itching, irritation. 2) Same symptoms as above occurred after the skin spot where you applied a product was exposed to direct sunlight. 2. Do not use for injured, eczema, or dermatitis spots. 3. Directions for storage and handling. 1) Remember to cover up a lid after using a product. 2) Keep a product in unreachable place from children. 3) Do not keep a product in too high or low temperature and under direct sunlight.

Reported adverse events (FAERS/openFDA)#

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