FDA.reportPublic FDA data

FDA label 8fa1498c-8b1d-4eb9-b7f8-a60bfeccbe7e

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
c65154a0-7389-4d3c-8370-6af038861623
SPL ID
8fa1498c-8b1d-4eb9-b7f8-a60bfeccbe7e
Version
2
Effective date
2018-11-26
Source export date
2026-09-28
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:22:17

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 Warnings: 1. Stop using if the following reactions occur at the contact area. Continuous use can worsen the reactions, so consult a dermatologist. If red spots, swelling, itchiness or irritations occur. If the above are observed in the area of application as a result of exposure to direct sunlight. 2. Do not apply if there is scratch, eczema or dermatitis on the skin. 3. Storage and Handling 1) Keep out of reach of children. 2) Keep out of high and low temperature and avoid exposure to direct sunlight.

Reported adverse events (FAERS/openFDA)#

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