NDC 0220-2165

Fucus vesiculosus

Fucus Vesiculosus

Fucus vesiculosus is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Boiron. The primary component is Fucus Vesiculosus.

• Product ID: 0220-2165_85a180d8-01d6-78b8-e053-2991aa0aed90
• NDC: 0220-2165
• Product Type: Human Otc Drug
• Proprietary Name: Fucus vesiculosus
• Generic Name: Fucus Vesiculosus
• Dosage Form: Pellet
• Route of Administration: ORAL
• Marketing Start Date: 1983-03-03
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Boiron
• Substance Name: FUCUS VESICULOSUS
• Active Ingredient Strength: 30 [hp_C]/30[hp_C]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 0220-2165-41

30 [hp_C] in 1 TUBE (0220-2165-41)

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

NDC SPL Data Element Entries

NDC 0220-2165-41 [00220216541]

Fucus vesiculosus PELLET

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

Drug Details

Active Ingredients

Ingredient	Strength
FUCUS VESICULOSUS	30 [hp_C]/30[hp_C]

OpenFDA Data

• SPL SET ID: 85a180d8-01d5-78b8-e053-2991aa0aed90
• Manufacturer:
  • Boiron
• UNII:
  • 535G2ABX9M

NDC Crossover Matching brand name "Fucus vesiculosus" or generic name "Fucus Vesiculosus"

NDC	Brand Name	Generic Name
0220-2165	Fucus vesiculosus	FUCUS VESICULOSUS
0220-2167	Fucus vesiculosus	FUCUS VESICULOSUS
15631-0199	FUCUS VESICULOSUS	FUCUS VESICULOSUS
15631-0587	FUCUS VESICULOSUS	FUCUS VESICULOSUS
57520-0676	Fucus Vesiculosus	Fucus vesiculosus,
60512-6695	FUCUS VESICULOSUS	FUCUS VESICULOSUS
68428-944	Fucus vesiculosus	FUCUS VESICULOSUS
71919-304	Fucus vesiculosus	FUCUS VESICULOSUS
58264-0106	D-100	Fucus vesiculosus