Package 0220-3389-41

Brand: mercurius sulphuratus ruber

Generic: mercuric sulfide
NDC Package

Package Facts

Identity

Package NDC 0220-3389-41
Digits Only 0220338941
Product NDC 0220-3389
Description

200 [kp_C] in 1 TUBE (0220-3389-41)

Marketing

Marketing Status
Marketed Since 2024-01-01
Brand mercurius sulphuratus ruber
Generic mercuric sulfide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "202328e9-612a-8bc4-e063-6394a90a827e", "openfda": {"unii": ["ZI0T668SF1"], "spl_set_id": ["202328e9-6129-8bc4-e063-6394a90a827e"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-3389-41)", "package_ndc": "0220-3389-41", "marketing_start_date": "20240101"}], "brand_name": "Mercurius sulphuratus ruber", "product_id": "0220-3389_202328e9-612a-8bc4-e063-6394a90a827e", "dosage_form": "PELLET", "product_ndc": "0220-3389", "generic_name": "MERCURIC SULFIDE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mercurius sulphuratus ruber", "active_ingredients": [{"name": "MERCURIC SULFIDE", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20240101", "listing_expiration_date": "20261231"}