NDC 58264-0092

D-86

Arnica Montana, Silicon Dioxide, Sodium Chloride, Lead Acetate Anhydrous, Selenicereus Grandiflorus Stem, Tribasic Calcium Phosphate, And Potassium Iodide

D-86 is a Sublingual Solution in the Human Otc Drug category. It is labeled and distributed by Dna Labs, Inc.. The primary component is Arnica Montana; Silicon Dioxide; Sodium Chloride; Lead Acetate Anhydrous; Selenicereus Grandiflorus Stem; Tribasic Calcium Phosphate; Potassium Iodide.

Product ID58264-0092_a3d2c559-5da3-4303-a463-acf993813997
NDC58264-0092
Product TypeHuman Otc Drug
Proprietary NameD-86
Generic NameArnica Montana, Silicon Dioxide, Sodium Chloride, Lead Acetate Anhydrous, Selenicereus Grandiflorus Stem, Tribasic Calcium Phosphate, And Potassium Iodide
Dosage FormSolution
Route of AdministrationSUBLINGUAL
Marketing Start Date1990-01-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameDNA Labs, Inc.
Substance NameARNICA MONTANA; SILICON DIOXIDE; SODIUM CHLORIDE; LEAD ACETATE ANHYDROUS; SELENICEREUS GRANDIFLORUS STEM; TRIBASIC CALCIUM PHOSPHATE; POTASSIUM IODIDE
Active Ingredient Strength30 [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 58264-0092-1

29.57 mL in 1 BOTTLE, GLASS (58264-0092-1)
Marketing Start Date1990-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 58264-0092-1 [58264009201]

D-86 SOLUTION
Marketing CategoryUnapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date1990-01-01
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
ARNICA MONTANA30 [hp_X]/mL

OpenFDA Data

SPL SET ID:54fa62d3-c129-4826-a794-f3dcc6b855bf
Manufacturer
UNII
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