FDA.reportPublic FDA data

FDA label 23fcb35e-e741-aeb1-e063-6394a90a23f7

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
209282e6-3699-fc54-e063-6294a90a5f1b
SPL ID
23fcb35e-e741-aeb1-e063-6394a90a23f7
Version
2
Effective date
2024-10-08
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 05:38:51

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

Warning: This product is not suitable for pregnant women and individuals with sensitive skin. Please use it only under medical guidance. Patients with damaged areas should not use this product. If skin itching or blisters occur after use, discontinue use or resume use after recovery. Do not use if the drug changes in consistency or texture. Children should only use it under the supervision of adults. If you are currently taking any other medications, consult a physician before using this product

Reported adverse events (FAERS/openFDA)#

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