NDC 60512-6695

FUCUS VESICULOSUS

Fucus Vesiculosus

FUCUS VESICULOSUS is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Homeolab Usa Inc.. The primary component is Fucus Vesiculosus.

• Product ID: 60512-6695_700fa09c-5049-427a-a655-a91b2281a9fd
• NDC: 60512-6695
• Product Type: Human Otc Drug
• Proprietary Name: FUCUS VESICULOSUS
• Generic Name: Fucus Vesiculosus
• Dosage Form: Pellet
• Route of Administration: ORAL
• Marketing Start Date: 2013-11-18
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: HOMEOLAB USA INC.
• Substance Name: FUCUS VESICULOSUS
• Active Ingredient Strength: 1 [hp_X]/1
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 60512-6695-1

80 PELLET in 1 TUBE (60512-6695-1)

• Marketing Start Date: 2013-11-18
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 60512-6695-1 [60512669501]

FUCUS VESICULOSUS PELLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2013-11-18
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
FUCUS VESICULOSUS	1 [hp_X]/1

OpenFDA Data

• SPL SET ID: 8f43f2a9-7038-4f1d-9249-93302f183b94
• Manufacturer:
  • HOMEOLAB USA INC.
• 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