TRIDERMA BRUISE DEFENSE HEALING -DIABETICS

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 BRUISE DEFENSE HEALING -DIABETICS
Generic name
ARNICA MONTANA FLOWER EXTRACT
Manufacturer
Genuine Virgin Aloe Corporation
Product type
HUMAN OTC DRUG
SPL set ID
6e772fc2-8ba6-4a6a-9856-ca70470a4f03
SPL ID
4977f4b0-cc80-a8a4-e063-6394a90a00a8
Version
5
Effective date
2026-01-28
Source export date
2026-09-28
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:25:50
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

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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 7 days or worsens. Keep out of 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.