NDC 58264-0046

D-46

Ferrosoferric Phosphate, Lithium Carbonate, Sodium Sulfate, Strychnos Nux-vomica Seed, Rhododendron Aureum Leaf, And Filipendula Ulmaria Root

D-46 is a Sublingual Solution in the Human Otc Drug category. It is labeled and distributed by Dna Labs, Inc.. The primary component is Ferrosoferric Phosphate; Lithium Carbonate; Sodium Sulfate; Strychnos Nux-vomica Seed; Rhododendron Aureum Leaf; Filipendula Ulmaria Root.

Product ID58264-0046_64481b91-2137-4645-ab41-521a1c023c3d
NDC58264-0046
Product TypeHuman Otc Drug
Proprietary NameD-46
Generic NameFerrosoferric Phosphate, Lithium Carbonate, Sodium Sulfate, Strychnos Nux-vomica Seed, Rhododendron Aureum Leaf, And Filipendula Ulmaria Root
Dosage FormSolution
Route of AdministrationSUBLINGUAL
Marketing Start Date1990-01-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameDNA Labs, Inc.
Substance NameFERROSOFERRIC PHOSPHATE; LITHIUM CARBONATE; SODIUM SULFATE; STRYCHNOS NUX-VOMICA SEED; RHODODENDRON AUREUM LEAF; FILIPENDULA ULMARIA ROOT
Active Ingredient Strength12 [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 58264-0046-1

29.57 mL in 1 BOTTLE, GLASS (58264-0046-1)
Marketing Start Date1990-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 58264-0046-1 [58264004601]

D-46 SOLUTION
Marketing CategoryUNAPPROVED HOMEOPATHIC
Product TypeHUMAN OTC DRUG
Marketing Start Date1990-01-01
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
FERROSOFERRIC PHOSPHATE12 [hp_X]/mL

OpenFDA Data

SPL SET ID:be8b4acb-83c6-4d25-ba90-ee6e6e0a588e
Manufacturer
UNII
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