TRIDERMA EVERYDAY BRUISE RELIEF

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: TRIDERMA EVERYDAY BRUISE RELIEF
Generic name: ARNICA MONTANA
Manufacturer: Genuine Virgin Aloe Corporation
Product type: HUMAN OTC DRUG
SPL set ID: 5100f2d0-cfa2-4136-bda4-860de81707c8
SPL ID: 497d62b9-309b-5d55-e063-6294a90a7e41
Version: 6
Effective date: 2026-01-28
Source export date: 2026-09-28
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/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:57:12

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 · 17 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		TRIDERMA EVERYDAY BRUISE RELIEF	openfda.brand_name
generic name		ARNICA MONTANA	openfda.generic_name
manufacturer name		Genuine Virgin Aloe Corporation	openfda.manufacturer_name
ndc	package	10738-059-50	openfda.package_ndc
ndc	package	10738-059-20	openfda.package_ndc
ndc	package	10738-059-41	openfda.package_ndc
ndc	package	10738-059-25	openfda.package_ndc
ndc	package	10738-059-55	openfda.package_ndc
ndc	product	10738-059	openfda.product_ndc
ndc11	package	10738005920	derived:openfda.package_ndc
ndc11	package	10738005955	derived:openfda.package_ndc
ndc11	package	10738005925	derived:openfda.package_ndc
ndc11	package	10738005950	derived:openfda.package_ndc
ndc11	package	10738005941	derived:openfda.package_ndc
spl id		497d62b9-309b-5d55-e063-6294a90a7e41	id
spl set id		5100f2d0-cfa2-4136-bda4-860de81707c8	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

Warnings For external use only. Avoid contact with eyes, mucous membranes, damaged skin and wounds. 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 or worsens. Keep out of the reach of children. If swallowed, get medical help and contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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