Arnica Montana 3X, 6X, 12X, 30X, 200X

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 Montana 3X, 6X, 12X, 30X, 200X
Generic name
ARNICA MONTANA ROOT
Manufacturer
MediNatura Inc
Product type
HUMAN OTC DRUG
SPL set ID
826f5ce1-b149-449f-b4dd-229e9ab4e40a
SPL ID
0a6b0e83-5280-4742-b415-a8404c2ec0e5
Version
3
Effective date
2022-08-18
Source export date
2026-10-12
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:48:07
Harmonized routes table
Harmonized routes
ORAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If symptoms persist or worsen, a health professional should be consulted. Do not use if sensitivity to Hendel Arnica montana 3X, 6X, 12X, 30X, 200X or any of its ingredients exists. In case of accidental overdose, contact a Poison Control Center immediately

Reported adverse events (FAERS/openFDA)#

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