FDA label 025a7556-d2d2-4c39-9609-b498209f0d62

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
65c1ed8e-7347-4cf4-82b3-9dd66c70bffd
SPL ID
025a7556-d2d2-4c39-9609-b498209f0d62
Version
5
Effective date
2025-11-20
Source export date
2026-10-12
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:46:07

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 When using this product Use only as directed Do not get into eyes or on mucous membranes Do not apply to wounds, damaged or irritated skin Do not bandage or cover with any type of wrap except clothing Do not use with a heating pad or apply external heat Do not use 1 hour prior to bathing or 30 minutes after bathing Stop use and ask a doctor if Condition worsens Severe skin irritation occurs Pain persists for more than 7 days If pregnant or breast-feeding, ask a healthcare professional before use. Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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