Package 0220-0629-41

Brand: aurum iodatum

Generic: gold monoiodide
NDC Package

Package Facts

Identity

Package NDC 0220-0629-41
Digits Only 0220062941
Product NDC 0220-0629
Description

200 [kp_C] in 1 TUBE (0220-0629-41)

Marketing

Marketing Status
Marketed Since 2025-01-01
Brand aurum iodatum
Generic gold monoiodide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "36c15b8e-012c-8638-e063-6294a90a4550", "openfda": {"unii": ["T1UDV7ES1A"], "spl_set_id": ["36c15b8e-012b-8638-e063-6294a90a4550"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-0629-41)", "package_ndc": "0220-0629-41", "marketing_start_date": "20250101"}], "brand_name": "AURUM IODATUM", "product_id": "0220-0629_36c15b8e-012c-8638-e063-6294a90a4550", "dosage_form": "PELLET", "product_ndc": "0220-0629", "generic_name": "GOLD MONOIODIDE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "AURUM IODATUM", "active_ingredients": [{"name": "GOLD MONOIODIDE", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20250101", "listing_expiration_date": "20261231"}