NDC 58264-0049

D-49

Arsenic Trioxide, Oyster Shell Calcium Carbonate, Crude, Mercuric Sulfide, Potassium Dichromate, Mercurius Solubilis, Anemone Pratensis, Sepia Officinalis Juice, And Sulfur

D-49 is a Sublingual Solution in the Human Otc Drug category. It is labeled and distributed by Dna Labs, Inc.. The primary component is Arsenic Trioxide; Oyster Shell Calcium Carbonate, Crude; Mercuric Sulfide; Potassium Dichromate; Mercurius Solubilis; Anemone Pratensis; Sepia Officinalis Juice; Sulfur.

Product ID58264-0049_4b3401e7-33f9-4e13-bfb0-06567ccd32ed
NDC58264-0049
Product TypeHuman Otc Drug
Proprietary NameD-49
Generic NameArsenic Trioxide, Oyster Shell Calcium Carbonate, Crude, Mercuric Sulfide, Potassium Dichromate, Mercurius Solubilis, Anemone Pratensis, Sepia Officinalis Juice, And Sulfur
Dosage FormSolution
Route of AdministrationSUBLINGUAL
Marketing Start Date1990-01-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameDNA Labs, Inc.
Substance NameARSENIC TRIOXIDE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; MERCURIC SULFIDE; POTASSIUM DICHROMATE; MERCURIUS SOLUBILIS; ANEMONE PRATENSIS; SEPIA OFFICINALIS JUICE; SULFUR
Active Ingredient Strength12 [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 FlagN
Listing Certified Through2019-12-31

Packaging

NDC 58264-0049-1

29.57 mL in 1 BOTTLE, GLASS (58264-0049-1)
Marketing Start Date1990-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 58264-0049-1 [58264004901]

D-49 SOLUTION
Marketing CategoryUNAPPROVED HOMEOPATHIC
Product TypeHUMAN OTC DRUG
Marketing Start Date1990-01-01
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
ARSENIC TRIOXIDE12 [hp_X]/mL

OpenFDA Data

SPL SET ID:26800b04-81c7-4094-afe8-4db6ca878f6d
Manufacturer
UNII
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