NDC 58264-0126

D-120

Calcium Fluoride, Bismuth Subnitrate, Zinc, Mercuric Chloride, Toxicodendron Pubescens Leaf, Antimony Trisulfide, Barium Carbonate, Echinacea Angustifolia, Iodine, Phosphoric Acid, Potassium Carbonate, Dibasic Potassium Phosphate, And Thuja Occidentalis Leafy Twig

D-120 is a Sublingual Solution in the Human Otc Drug category. It is labeled and distributed by Dna Labs, Inc.. The primary component is Calcium Fluoride; Bismuth Subnitrate; Zinc; Mercuric Chloride; Toxicodendron Pubescens Leaf; Antimony Trisulfide; Barium Carbonate; Echinacea Angustifolia; Iodine; Phosphoric Acid; Potassium Carbonate; Dibasic Potassium Phosphate; Thuja Occidentalis Leafy Twig.

Product ID58264-0126_a40aac38-9cf4-4cd8-9519-7f3ec70ee4a5
NDC58264-0126
Product TypeHuman Otc Drug
Proprietary NameD-120
Generic NameCalcium Fluoride, Bismuth Subnitrate, Zinc, Mercuric Chloride, Toxicodendron Pubescens Leaf, Antimony Trisulfide, Barium Carbonate, Echinacea Angustifolia, Iodine, Phosphoric Acid, Potassium Carbonate, Dibasic Potassium Phosphate, And Thuja Occidentalis Leafy Twig
Dosage FormSolution
Route of AdministrationSUBLINGUAL
Marketing Start Date1990-01-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameDNA Labs, Inc.
Substance NameCALCIUM FLUORIDE; BISMUTH SUBNITRATE; ZINC; MERCURIC CHLORIDE; TOXICODENDRON PUBESCENS LEAF; ANTIMONY TRISULFIDE; BARIUM CARBONATE; ECHINACEA ANGUSTIFOLIA; IODINE; PHOSPHORIC ACID; POTASSIUM CARBONATE; DIBASIC POTASSIUM PHOSPHATE; THUJA OCCIDENTALIS LEAFY TWIG
Active Ingredient Strength8 [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; [hp_X]/mL; [hp_X]/mL
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 58264-0126-1

29.57 mL in 1 BOTTLE, GLASS (58264-0126-1)
Marketing Start Date1990-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 58264-0126-1 [58264012601]

D-120 SOLUTION
Marketing CategoryUNAPPROVED HOMEOPATHIC
Product TypeHUMAN OTC DRUG
Marketing Start Date1990-01-01
Inactivation Date2020-01-31

Drug Details


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