FDA label 5a1180c5-2b12-fbce-e063-6294a90a5443

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
49e2af07-a634-d1ea-e063-6394a90ae0f0
SPL ID
5a1180c5-2b12-fbce-e063-6294a90a5443
Version
2
Effective date
2026-08-27
Source export date
2026-09-28
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:26:49

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

∙Avoid contract with towels or friction while bathing or showering after application to prevent the patch from peeling off. ∙After application, detoxification effects may cause body impurities to be released and transferred onto clothing always wear undergarments over the applied area. ∙Temporary symptoms such as itching, tingling, or mild pain may occur after application and typically subside within a few days, depending on individual conditions.

Reported adverse events (FAERS/openFDA)#

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