FDA label d85fdb20-035a-41f8-a723-24ec2f8b1e68

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
059a34dc-b08e-42d3-89e3-84d5908c92a3
SPL ID
d85fdb20-035a-41f8-a723-24ec2f8b1e68
Version
1
Effective date
2021-09-24
Source export date
2026-09-28
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:13:48

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.