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: 2026-09-28
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/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:15:15

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 9 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Arnica Bruise Cream	openfda.brand_name
generic name		ARNICA MONTANA	openfda.generic_name
manufacturer name		Beautivity LLC	openfda.manufacturer_name
ndc	package	85398-005-01	openfda.package_ndc
ndc	product	85398-005	openfda.product_ndc
ndc11	package	85398000501	derived:openfda.package_ndc
spl id		5566eb74-e126-fe91-e063-6294a90a47e6	id
spl set id		348f3161-8abf-26d7-e063-6294a90a41dc	set_id
unii		O80TY208ZW	openfda.unii

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.

Reported adverse events (FAERS/openFDA)#

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