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: 2026-09-28
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/2026-09-28/db99fd80353afecef4949b48edcaa018be72b966b2360184251eb14df43743f9/drug-label-0014-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:40:01

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		Dr.Johnes Arnica Bruise Arnica Montana 1X HPUS (7%)	openfda.brand_name
generic name		ARNICA MONTANA 1X HPUS (7%)	openfda.generic_name
manufacturer name		Dr.Johnes LLC	openfda.manufacturer_name
ndc	package	85818-006-01	openfda.package_ndc
ndc	product	85818-006	openfda.product_ndc
ndc11	package	85818000601	derived:openfda.package_ndc
spl id		bcd5501e-49bb-4b5d-abdc-5cc7e86f9306	id
spl set id		4692f742-6225-4b6c-ae70-accd34c64f73	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 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.

Reported adverse events (FAERS/openFDA)#

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