NDC 58264-0075

D-75

Caulophyllum Thalictroides Root, Matricaria Chamomilla, Black Cohosh, Cupric Acetate, Magnesium Phosphate, Dibasic Trihydrate, And Viburnum Opulus Bark

D-75 is a Sublingual Solution in the Human Otc Drug category. It is labeled and distributed by Dna Labs, Inc.. The primary component is Caulophyllum Thalictroides Root; Matricaria Chamomilla; Black Cohosh; Cupric Acetate; Magnesium Phosphate, Dibasic Trihydrate; Viburnum Opulus Bark.

• Product ID: 58264-0075_b8f44ba4-640c-4f52-823f-5e8a0c860472
• NDC: 58264-0075
• Product Type: Human Otc Drug
• Proprietary Name: D-75
• Generic Name: Caulophyllum Thalictroides Root, Matricaria Chamomilla, Black Cohosh, Cupric Acetate, Magnesium Phosphate, Dibasic Trihydrate, And Viburnum Opulus Bark
• 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: CAULOPHYLLUM THALICTROIDES ROOT; MATRICARIA CHAMOMILLA; BLACK COHOSH; CUPRIC ACETATE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; VIBURNUM OPULUS BARK
• Active Ingredient Strength: 3 [hp_X]/mL; [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 58264-0075-1

29.57 mL in 1 BOTTLE, GLASS (58264-0075-1)

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

NDC SPL Data Element Entries

NDC 58264-0075-1 [58264007501]

D-75 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
CAULOPHYLLUM THALICTROIDES ROOT	3 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 28558d59-8e55-4a72-8d42-de3f54d4ebbb
• Manufacturer:
  • DNA Labs, Inc.
• UNII:
  • 39M11XPH03
  • JTJ6HH6YEH
  • T1UG6H6805
  • K73E24S6X9
  • G0R4UBI2ZZ
  • HF539G9L3Q