FDA.reportPublic FDA data

FDA label 61758a62-e741-4585-94d5-414dcd1cab46

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
f4c58c16-b1cb-46f3-a4cd-3008885daf53
SPL ID
61758a62-e741-4585-94d5-414dcd1cab46
Version
2
Effective date
2018-10-26
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 05:41:52

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 For external use only Do not use • on wounds • damaged or irritated skin • heating pad or device • 30 min prior or after bathing Ask a doctor before use if you have • sensitive skin When using this product • avoid contact with the eyes or mucous membranes • do not bandage tightly Stop use and ask a doctor if • condition worsens • pain persists for more than 7 days or clear up and recur a few days later • severe skin irritation occur If pregnant or breast-feeding • ask a health professional before use

Reported adverse events (FAERS/openFDA)#

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