NDC 58264-0040

D-40

Phosphoric Acid, Lycopodium Clavatum Spore, Sodium Sulfate, Claviceps Purpurea Sclerotium, Uranyl Nitrate Hexahydrate, Phaseolus Vulgaris Whole, And Arsenic Trioxide

D-40 is a Sublingual Solution in the Human Otc Drug category. It is labeled and distributed by Dna Labs, Inc.. The primary component is Phosphoric Acid; Lycopodium Clavatum Spore; Sodium Sulfate; Claviceps Purpurea Sclerotium; Uranyl Nitrate Hexahydrate; Phaseolus Vulgaris Whole; Arsenic Trioxide.

Product ID58264-0040_2ed02b7a-81a5-4f60-916e-ab2cba05b140
NDC58264-0040
Product TypeHuman Otc Drug
Proprietary NameD-40
Generic NamePhosphoric Acid, Lycopodium Clavatum Spore, Sodium Sulfate, Claviceps Purpurea Sclerotium, Uranyl Nitrate Hexahydrate, Phaseolus Vulgaris Whole, And Arsenic Trioxide
Dosage FormSolution
Route of AdministrationSUBLINGUAL
Marketing Start Date1990-01-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameDNA Labs, Inc.
Substance NamePHOSPHORIC ACID; LYCOPODIUM CLAVATUM SPORE; SODIUM SULFATE; CLAVICEPS PURPUREA SCLEROTIUM; URANYL NITRATE HEXAHYDRATE; PHASEOLUS VULGARIS WHOLE; ARSENIC TRIOXIDE
Active Ingredient Strength12 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 58264-0040-1

29.57 mL in 1 BOTTLE, GLASS (58264-0040-1)
Marketing Start Date1990-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 58264-0040-1 [58264004001]

D-40 SOLUTION
Marketing CategoryUnapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date1990-01-01
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
PHOSPHORIC ACID12 [hp_X]/mL

OpenFDA Data

SPL SET ID:8a86c0ee-93e9-48da-a7d8-89225e233177
Manufacturer
UNII
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