FDA.reportPublic FDA data

Arnica Bruise Cream

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)

Brand name
Arnica Bruise Cream
Generic name
ARNICA MONTANA
Manufacturer
Beautivity LLC
Product type
HUMAN OTC DRUG
SPL set ID
348f3161-8abf-26d7-e063-6294a90a41dc
SPL ID
5566eb74-e126-fe91-e063-6294a90a47e6
Version
3
Effective date
2026-06-29
Source export date
2026-08-01
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/2026-08-01/5cbbf4af8f4e275ec50931155b30ffa7322568b9af8a1c936a47f6d6774862fd/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:01:54
Harmonized routes table
Harmonized routes
TOPICAL

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. if you are allergic to Arnica Montana or any inactive ingredients in 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 a doctor if: Condition persists for more than 3 days or worsens. Symptoms clear up and occur again within a few days If swallowed, get medical help or contact a Poison Control Center right away.