FDA label 36986359-867e-49a7-bbdd-9101edd4366b

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
36986359-867e-49a7-bbdd-9101edd4366b
SPL ID
36986359-867e-49a7-bbdd-9101edd4366b
Version
1
Effective date
2013-05-27
Source export date
2026-09-28
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:41:53

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

1. If you experience following occasions after using this product, stop using. If your symptom got worse, have a consultation with dermatologist. 1) When you have problems such as red spots, swelling, itching, and stimulus 2) If applied parts have problems like above due to direct ray of light 2. Do not use for the parts with wound, eczema, and dermatitis. 3. Suggestions in regard of keeping and treatment 1) Make sure to close the stopper after using 2) Keep it in the place where infants or children's hands do not reach 3) Do not keep it in the place with high and low temperature and sunlight touches

Reported adverse events (FAERS/openFDA)#

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