FDA.reportPublic FDA data

FDA label 1e7ab4e4-ef65-d71c-e063-6394a90ac5d8

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
1e7ab4e4-ef64-d71c-e063-6394a90ac5d8
SPL ID
1e7ab4e4-ef65-d71c-e063-6394a90ac5d8
Version
1
Effective date
2024-08-01
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 05:25:41

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

For External Use Only Do not use on wounds - damaged, broken, or irritated skin Stop use and ask doctor if condition worsens * irritation develops *redness is present *symptoms persist for more than 7 days or clear up and occur again within a few days ______________________________ When using this product Use only as directed Avoid contact with eyes or mucous membranes Do not bandage tightly or use with a heating pad. ______________________________ 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.