FDA label bef58e18-1dfa-39ed-e053-2995a90a763d

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
bebe47ec-f7a8-8fee-e053-2a95a90a02f6
SPL ID
bef58e18-1dfa-39ed-e053-2995a90a763d
Version
3
Effective date
2021-04-01
Source export date
2026-09-28
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:52:15

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. Consult a physician if red spots, swollenness, itchiness, or any other abnormal symptoms or side effects develops on the applied area during or after use or under direct sunlight. 2. Do not use on wound, etc. 3. Precautions for handling and storage a) Keep out of the reach of children b) Avoid direct sunlight

Reported adverse events (FAERS/openFDA)#

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