FDA label c0a93d9b-3313-451a-bf58-887cb3a9591f

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
393f98a9-48c6-462f-81ed-4b8f92feb221
SPL ID
c0a93d9b-3313-451a-bf58-887cb3a9591f
Version
4
Effective date
2018-08-24
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 01:29:56

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 ​​ Allergy Alert Do not use if you are allergic to Arnica montana or to any of this product's inactive ingredients When using this product use only as directed do not bandage tightly or use a heating pad Stop use and ask a doctor if condition persists for more than 3 days condition worsens Keep out of reach of children. ​If swallowed, ​get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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