NDC 0220-2850

Kali arsenicosum

Potassium Arsenite Anhydrous

Kali arsenicosum is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Boiron. The primary component is Potassium Arsenite Anhydrous.

• Product ID: 0220-2850_68f7f674-657e-6890-e053-2991aa0ae8a6
• NDC: 0220-2850
• Product Type: Human Otc Drug
• Proprietary Name: Kali arsenicosum
• Generic Name: Potassium Arsenite Anhydrous
• Dosage Form: Pellet
• Route of Administration: ORAL
• Marketing Start Date: 1983-03-03
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Boiron
• Substance Name: POTASSIUM ARSENITE ANHYDROUS
• Active Ingredient Strength: 30 [hp_C]/30[hp_C]
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 0220-2850-41

30 [hp_C] in 1 TUBE (0220-2850-41)

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

NDC SPL Data Element Entries

NDC 0220-2850-41 [00220285041]

Kali arsenicosum PELLET

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

Drug Details

Active Ingredients

Ingredient	Strength
POTASSIUM ARSENITE ANHYDROUS	30 [hp_C]/30[hp_C]

OpenFDA Data

• SPL SET ID: 68f7f674-657d-6890-e053-2991aa0ae8a6
• Manufacturer:
  • Boiron
• UNII:
  • BM2U42PAKI

NDC Crossover Matching brand name "Kali arsenicosum" or generic name "Potassium Arsenite Anhydrous"

NDC	Brand Name	Generic Name
0220-2847	Kali arsenicosum	POTASSIUM ARSENITE ANHYDROUS
0220-2850	Kali arsenicosum	POTASSIUM ARSENITE ANHYDROUS
15631-0246	KALI ARSENICOSUM	KALI ARSENICOSUM
15631-0607	KALI ARSENICOSUM	KALI ARSENICOSUM
68428-448	Kali arsenicosum	POTASSIUM ARSENITE ANHYDROUS
71919-377	Kali arsenicosum	POTASSIUM ARSENITE ANHYDROUS