NDC 58264-0002

D2

Gold Trichloride, Crataegus Laevigata Whole, Selenicereus Grandiflorus Whole, Dibasic Potassium Phosphate, Aconitum Napellus, Valeriana Officinalis Whole, Spigelia Anthelmia, Arnica Montana, Digitalis Purpurea Whole, Prunus Laurocerasus Whole, And Strychnos Ignatii Whole

D2 is a Sublingual Solution in the Human Otc Drug category. It is labeled and distributed by Dna Labs, Inc.. The primary component is Gold Trichloride; Crataegus Laevigata Whole; Selenicereus Grandiflorus Whole; Dibasic Potassium Phosphate; Aconitum Napellus; Valeriana Officinalis Whole; Spigelia Anthelmia; Arnica Montana; Digitalis Purpurea Whole; Prunus Laurocerasus Whole; Strychnos Ignatii Whole.

• Product ID: 58264-0002_908e4ffc-c159-41ba-97ff-5e972fb82195
• NDC: 58264-0002
• Product Type: Human Otc Drug
• Proprietary Name: D2
• Generic Name: Gold Trichloride, Crataegus Laevigata Whole, Selenicereus Grandiflorus Whole, Dibasic Potassium Phosphate, Aconitum Napellus, Valeriana Officinalis Whole, Spigelia Anthelmia, Arnica Montana, Digitalis Purpurea Whole, Prunus Laurocerasus Whole, And Strychnos Ignatii Whole
• 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: GOLD TRICHLORIDE; CRATAEGUS LAEVIGATA WHOLE; SELENICEREUS GRANDIFLORUS WHOLE; DIBASIC POTASSIUM PHOSPHATE; ACONITUM NAPELLUS; VALERIANA OFFICINALIS WHOLE; SPIGELIA ANTHELMIA; ARNICA MONTANA; DIGITALIS PURPUREA WHOLE; PRUNUS LAUROCERASUS WHOLE; STRYCHNOS IGNATII WHOLE
• Active Ingredient Strength: 6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [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 58264-0002-1

29.57 mL in 1 BOTTLE, GLASS (58264-0002-1)

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

NDC SPL Data Element Entries

NDC 58264-0002-1 [58264000201]

D2 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
GOLD TRICHLORIDE	6 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 146b1277-28c3-43e3-877b-13b324717d2a
• Manufacturer:
  • DNA Labs, Inc.
• UNII:
  • WYT05213GE
  • EFX9G567MJ
  • O80TY208ZW
  • 6YSJ329777
  • X8H7HS7MRM
  • CI71S98N1Z
  • 15443PR153
  • FP6O7F1X9R
  • 516S28LU0T
  • UD4O8TY7RW
  • U0NQ8555JD