NDC 58264-0037

D-37

Aluminum Oxide, Bryonia Alba Root, Citrullus Colocynthis Fruit Pulp, Lachesis Muta Venom, Lycopodium Clavatum Spore, Mercuric Chloride, Strychnos Nux-vomica Seed, Lead Acetate Anhydrous, And Sulfur

D-37 is a Sublingual Solution in the Human Otc Drug category. It is labeled and distributed by Dna Labs, Inc.. The primary component is Aluminum Oxide; Bryonia Alba Root; Citrullus Colocynthis Fruit Pulp; Lachesis Muta Venom; Lead Acetate Anhydrous; Lycopodium Clavatum Spore; Mercuric Chloride; Strychnos Nux-vomica Seed; Sulfur.

Product ID58264-0037_e083159f-a6c7-240a-e053-2995a90a7c6c
NDC58264-0037
Product TypeHuman Otc Drug
Proprietary NameD-37
Generic NameAluminum Oxide, Bryonia Alba Root, Citrullus Colocynthis Fruit Pulp, Lachesis Muta Venom, Lycopodium Clavatum Spore, Mercuric Chloride, Strychnos Nux-vomica Seed, Lead Acetate Anhydrous, And Sulfur
Dosage FormSolution
Route of AdministrationSUBLINGUAL
Marketing Start Date1990-01-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameDNA Labs, Inc.
Substance NameALUMINUM OXIDE; BRYONIA ALBA ROOT; CITRULLUS COLOCYNTHIS FRUIT PULP; LACHESIS MUTA VENOM; LEAD ACETATE ANHYDROUS; LYCOPODIUM CLAVATUM SPORE; MERCURIC CHLORIDE; STRYCHNOS NUX-VOMICA SEED; 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; [hp_X]/mL
Pharm ClassesAllergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 58264-0037-1

29.57 mL in 1 BOTTLE, GLASS (58264-0037-1)
Marketing Start Date1990-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 58264-0037-1 [58264003701]

D-37 SOLUTION
Marketing CategoryUNAPPROVED HOMEOPATHIC
Product TypeHUMAN OTC DRUG
Marketing Start Date1990-01-01
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
ALUMINUM OXIDE12 [hp_X]/mL

OpenFDA Data

SPL SET ID:3b408532-b84b-4398-ab8d-64d5a9c8d092
Manufacturer
UNII

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