arnica montana
Generic: arnica montana
Labeler: boironDrug Facts
Product Profile
Brand Name
arnica montana
Generic Name
arnica montana
Labeler
boiron
Dosage Form
PELLET
Routes
Active Ingredients
arnica montana 12 [hp_X]/12[hp_X]
Manufacturer
Identifiers & Regulatory
Product NDC
0220-0449
Product ID
0220-0449_471d8d0e-8753-5063-e063-6394a90a2dcc
Product Type
HUMAN OTC DRUG
Marketing Category
UNAPPROVED HOMEOPATHIC
Listing Expiration
2026-12-31
Marketing Start
1983-03-03
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
02200449
Hyphenated Format
0220-0449
Supplemental Identifiers
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
arnica montana (source: ndc)
Generic Name
arnica montana (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 12 [hp_X]/12[hp_X]
Packaging
- 12 [hp_X] in 1 TUBE (0220-0449-41)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "471d8d0e-8753-5063-e063-6394a90a2dcc", "openfda": {"unii": ["O80TY208ZW"], "spl_set_id": ["84eebf11-d58c-1e9f-e053-2991aa0a9cf3"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 [hp_X] in 1 TUBE (0220-0449-41)", "package_ndc": "0220-0449-41", "marketing_start_date": "19830303"}], "brand_name": "Arnica montana", "product_id": "0220-0449_471d8d0e-8753-5063-e063-6394a90a2dcc", "dosage_form": "PELLET", "product_ndc": "0220-0449", "generic_name": "ARNICA MONTANA", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Arnica montana", "active_ingredients": [{"name": "ARNICA MONTANA", "strength": "12 [hp_X]/12[hp_X]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}