FDA.reportPublic FDA data

FDA label 19e6f005-58b1-416b-a6ab-7e0340cb9e20

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
4a9ea13a-87a7-41aa-9000-49c56e7c0363
SPL ID
19e6f005-58b1-416b-a6ab-7e0340cb9e20
Version
2
Effective date
2015-02-01
Source export date
2026-10-12
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:30:19

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 • On infected or damaged skin • While exercising or performing sweaty activities (yoga, swimming, and etc.,) When using this product: • Avoid contact with eyes or mouth • Do not bandage tightly Stop use and ask a doctor if: • Condition worsens • Symptom clear up and occur again within a few days. • Symptom persist for more than 7 days. • Nausea, vomiting, abdominal discomfort, diarrhea, or skin rash occurs. • Excessive irritation of the skin develops

Reported adverse events (FAERS/openFDA)#

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