Arnica Montana 30C HPUS

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 30C HPUS
Generic name: ARNICA MONTANA
Manufacturer: VITAMEDICA, INC.
Product type: HUMAN OTC DRUG
SPL set ID: 3d6bfff9-16a2-8ff8-e063-6394a90a2bda
SPL ID: 4e580e93-09b7-ad67-e063-6394a90aea01
Version: 2
Effective date: 2026-03-31
Source export date: 2026-11-06
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/2026-11-06/9d5577a314a25811fefbde4767c9b37f3913d9a65fdc458c6336b5aed532339e/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
Import run: 20261106T075659Z
Imported at: 2026-11-06 08:52:29

Harmonized routes table
Harmonized routes
ORAL

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Arnica Montana 30C HPUS	openfda.brand_name
generic name		ARNICA MONTANA	openfda.generic_name
manufacturer name		VITAMEDICA, INC.	openfda.manufacturer_name
ndc	package	80004-300-20	openfda.package_ndc
ndc	package	80004-300-10	openfda.package_ndc
ndc	product	80004-300	openfda.product_ndc
ndc11	package	80004030010	derived:openfda.package_ndc
ndc11	package	80004030020	derived:openfda.package_ndc
spl id		4e580e93-09b7-ad67-e063-6394a90aea01	id
spl set id		3d6bfff9-16a2-8ff8-e063-6394a90a2bda	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: Ask a doctor before use if pregnant or breastfeeding. Stop use or consult a physician if • Any adverse reactions occur • Symptoms persist for more than 14-days or worsen Discontinue use if any adverse reactions occur. Keep this and all medications out of reach of children. In case of an emergency or accidental overdose, contact a medical professional or Poison Control immediately.

Reported adverse events (FAERS/openFDA)#

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