FDA label f27ab7ec-8a14-7dd7-e053-2a95a90aa93a

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
f27ab7ec-8a13-7dd7-e053-2a95a90aa93a
SPL ID
f27ab7ec-8a14-7dd7-e053-2a95a90aa93a
Version
1
Effective date
2023-01-17
Source export date
2026-08-01
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/206e0852f7011b53c21719ec5c68ac6752381d0fcd1d348f7428adad64429e89/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:18:01

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 if you are allergic to Arnica montana or to any of this product's inactive ingredients. When using this product avoid contact with eyes, mucous membranes, wounds, damaged or irritated skin use only as directed do not tightly wrap or bandage the treated area do not apply heat or ice to the treated area immediately before or after use Stop use and ask doctor if condition persists for more than 3 days or worsens symptoms clear up and occur again within a few days If pregnant or breastfeeding, consult a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.