Package 0220-0541-41

Brand: arnica montana radix

Generic: arnica montana root
NDC Package

Package Facts

Identity

Package NDC 0220-0541-41
Digits Only 0220054141
Product NDC 0220-0541
Description

200 [kp_C] in 1 TUBE (0220-0541-41)

Marketing

Marketing Status
Marketed Since 2024-01-01
Brand arnica montana radix
Generic arnica montana root
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "15487722-c402-c601-e063-6294a90a3ae0", "openfda": {"unii": ["MUE8Y11327"], "spl_set_id": ["1547f6d8-d0b5-466b-e063-6294a90ab875"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-0541-41)", "package_ndc": "0220-0541-41", "marketing_start_date": "20240101"}], "brand_name": "Arnica montana radix", "product_id": "0220-0541_15487722-c402-c601-e063-6294a90a3ae0", "dosage_form": "PELLET", "product_ndc": "0220-0541", "generic_name": "ARNICA MONTANA ROOT", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Arnica montana radix", "active_ingredients": [{"name": "ARNICA MONTANA ROOT", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20240101", "listing_expiration_date": "20261231"}