NDC 58264-0010

D-10

Sepia Officinalis Whole, Sanguinaria Canadensis Root, Sulfuric Acid, Black Cohosh, And Lachesis Muta Venom

D-10 is a Sublingual Solution in the Human Otc Drug category. It is labeled and distributed by Dna Labs, Inc.. The primary component is Sepia Officinalis Whole; Sanguinaria Canadensis Root; Sulfuric Acid; Black Cohosh; Lachesis Muta Venom.

• Product ID: 58264-0010_2e8eb1b7-db4f-4958-a1cb-3094226c55c3
• NDC: 58264-0010
• Product Type: Human Otc Drug
• Proprietary Name: D-10
• Generic Name: Sepia Officinalis Whole, Sanguinaria Canadensis Root, Sulfuric Acid, Black Cohosh, And Lachesis Muta Venom
• 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: SEPIA OFFICINALIS WHOLE; SANGUINARIA CANADENSIS ROOT; SULFURIC ACID; BLACK COHOSH; LACHESIS MUTA VENOM
• Active Ingredient Strength: 4 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 58264-0010-1

29.57 mL in 1 BOTTLE, GLASS (58264-0010-1)

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

NDC SPL Data Element Entries

NDC 58264-0010-1 [58264001001]

D-10 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
SEPIA OFFICINALIS WHOLE	4 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 1e5ba502-eef4-4df0-8330-b70d1872b4bb
• Manufacturer:
  • DNA Labs, Inc.
• UNII:
  • K73E24S6X9
  • N9288CD508
  • 48GD5780QF
  • VSW71SS07I
  • O40UQP6WCF