FDA.reportPublic FDA data

Dr.Johnes Arnica Bruise Arnica Montana 1X HPUS (7%)

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
Dr.Johnes Arnica Bruise Arnica Montana 1X HPUS (7%)
Generic name
ARNICA MONTANA 1X HPUS (7%)
Manufacturer
Dr.Johnes LLC
Product type
HUMAN OTC DRUG
SPL set ID
4692f742-6225-4b6c-ae70-accd34c64f73
SPL ID
bcd5501e-49bb-4b5d-abdc-5cc7e86f9306
Version
2
Effective date
2025-07-19
Source export date
2026-08-17
Source partition
14
Source file
https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-17/6bd7d3c0eada4b79bee746b510c338b1fde9a77f0accb4d86e3da2de4f0838aa/drug-label-0014-of-0014.json.zip
Source manifest SHA-256
ca19d5b1416b6b66a9d383bfdc77d90e91adfeefe16ffcc1ac6b06ceb90d8d73
Import run
20260818T065550Z
Imported at
2026-08-18 08:44:56
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 Do not apply to broken skin or open wounds. Avoid contact with eyes. When using this product Avoid contact with eyes. Stop use and ask a doctor if Condition worsens Symptoms persist for more than 7 days or clear up and occur again within a few days. If pregnant or breast-feeding Ask a health professional before use Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.