Package 0220-0518-41

Brand: arnica montana radix

Generic: arnica montana root
NDC Package

Package Facts

Identity

Package NDC 0220-0518-41
Digits Only 0220051841
Product NDC 0220-0518
Description

30 [hp_C] in 1 TUBE (0220-0518-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
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": "1547c3d2-028f-2d95-e063-6294a90a0fb4", "openfda": {"unii": ["MUE8Y11327"], "spl_set_id": ["8422bad4-ef04-e596-e053-2991aa0a81d3"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_C] in 1 TUBE (0220-0518-41)", "package_ndc": "0220-0518-41", "marketing_start_date": "19830303"}], "brand_name": "Arnica montana radix", "product_id": "0220-0518_1547c3d2-028f-2d95-e063-6294a90a0fb4", "dosage_form": "PELLET", "product_ndc": "0220-0518", "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": "30 [hp_C]/30[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}