NDC 0220-0632

Aurum iodatum

Gold Monoiodide

Aurum iodatum is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Boiron. The primary component is Gold Monoiodide.

• Product ID: 0220-0632_6c40ea02-4077-3880-e053-2991aa0ad6c1
• NDC: 0220-0632
• Product Type: Human Otc Drug
• Proprietary Name: Aurum iodatum
• Generic Name: Gold Monoiodide
• Dosage Form: Pellet
• Route of Administration: ORAL
• Marketing Start Date: 1983-03-03
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Boiron
• Substance Name: GOLD MONOIODIDE
• Active Ingredient Strength: 6 [hp_C]/6[hp_C]
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 0220-0632-41

6 [hp_C] in 1 TUBE (0220-0632-41)

• Marketing Start Date: 1983-03-03
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0220-0632-41 [00220063241]

Aurum iodatum PELLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1983-03-03

Drug Details

Active Ingredients

Ingredient	Strength
GOLD MONOIODIDE	6 [hp_C]/6[hp_C]

OpenFDA Data

• SPL SET ID: 6c40ea02-4076-3880-e053-2991aa0ad6c1
• Manufacturer:
  • Boiron
• UNII:
  • T1UDV7ES1A

NDC Crossover Matching brand name "Aurum iodatum" or generic name "Gold Monoiodide"

NDC	Brand Name	Generic Name
0220-0630	Aurum iodatum	GOLD MONOIODIDE
0220-0632	Aurum iodatum	GOLD MONOIODIDE
15631-0064	AURUM IODATUM	AURUM IODATUM
68428-239	Aurum iodatum	GOLD MONOIODIDE
71919-100	Aurum iodatum	GOLD MONOIODIDE