NDC 58264-0106

D-100

Fucus Vesiculosus

D-100 is a Sublingual Solution in the Human Otc Drug category. It is labeled and distributed by Dna Labs, Inc.. The primary component is Fucus Vesiculosus.

• Product ID: 58264-0106_dc71203a-e92b-480c-8fdb-69b55cdc69ee
• NDC: 58264-0106
• Product Type: Human Otc Drug
• Proprietary Name: D-100
• Generic Name: Fucus Vesiculosus
• Dosage Form: Solution
• Route of Administration: SUBLINGUAL
• Marketing Start Date: 1990-01-01
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: DNA Labs, Inc.
• Substance Name: FUCUS VESICULOSUS
• Active Ingredient Strength: 3 [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 58264-0106-1

29.57 mL in 1 BOTTLE, GLASS (58264-0106-1)

• Marketing Start Date: 1990-01-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 58264-0106-1 [58264010601]

D-100 SOLUTION

• Marketing Category: UNAPPROVED HOMEOPATHIC
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1990-01-01
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
FUCUS VESICULOSUS	3 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 0a2aed6f-6e1c-43e4-b5df-1dc73d7e6f2b
• Manufacturer:
  • DNA Labs, Inc.
• UNII:
  • 535G2ABX9M

NDC Crossover Matching brand name "D-100" or generic name "Fucus Vesiculosus"

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