FDA label 52195170-8e8a-4632-bb09-3fdedddd16ec

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
1e686ff1-1c0b-4c67-87fa-7f06e7d3bce1
SPL ID
52195170-8e8a-4632-bb09-3fdedddd16ec
Version
1
Effective date
2020-11-09
Source export date
2026-09-28
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:31:27

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. If any red spot, swelling, itchiness, or skin irritation develops after using the product or if direct sunlight causes irritation, stop using and consult a doctor. 2. Do not apply on areas with scars, eczema, or dermatitis. 3. Caution for storage and treatment. 1) Keep out of children's reach. 2) Avoid storing in areas exposed to direct sunlight.

Reported adverse events (FAERS/openFDA)#

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