Package 0220-9083-04

Brand: arnicare bruise

Generic: arnica montana
NDC Package

Package Facts

Identity

Package NDC 0220-9083-04
Digits Only 0220908304
Product NDC 0220-9083
Description

60 TABLET in 1 BLISTER PACK (0220-9083-04)

Marketing

Marketing Status
Marketed Since 2022-01-18
Brand arnicare bruise
Generic arnica montana
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "39fc5ac1-2ea9-12b9-e063-6394a90af459", "openfda": {"upc": ["0306969083048"], "unii": ["O80TY208ZW"], "spl_set_id": ["d5e1a96c-4a19-c58c-e053-2a95a90aca9e"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BLISTER PACK (0220-9083-04)", "package_ndc": "0220-9083-04", "marketing_start_date": "20220118"}], "brand_name": "Arnicare Bruise", "product_id": "0220-9083_39fc5ac1-2ea9-12b9-e063-6394a90af459", "dosage_form": "TABLET", "product_ndc": "0220-9083", "generic_name": "ARNICA MONTANA", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Arnicare Bruise", "active_ingredients": [{"name": "ARNICA MONTANA", "strength": "9 [hp_C]/1"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20220118", "listing_expiration_date": "20261231"}