aurum iodatum
Generic: gold monoiodide
Labeler: boironDrug Facts
Product Profile
Brand Name
aurum iodatum
Generic Name
gold monoiodide
Labeler
boiron
Dosage Form
PELLET
Routes
Active Ingredients
gold monoiodide 200 [kp_C]/200[kp_C]
Manufacturer
Identifiers & Regulatory
Product NDC
0220-0629
Product ID
0220-0629_36c15b8e-012c-8638-e063-6294a90a4550
Product Type
HUMAN OTC DRUG
Marketing Category
UNAPPROVED HOMEOPATHIC
Listing Expiration
2026-12-31
Marketing Start
2025-01-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
02200629
Hyphenated Format
0220-0629
Supplemental Identifiers
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
aurum iodatum (source: ndc)
Generic Name
gold monoiodide (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 [kp_C]/200[kp_C]
Packaging
- 200 [kp_C] in 1 TUBE (0220-0629-41)
Packages (1)
Ingredients (1)
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"}