NDC 58264-0219

N-21

Calcium Fluoride, Silicon Dioxide, Euphrasia Stricta, Ruta Graveolens Whole, Gelsemium Sempervirens Whole, Physostigma Venenosum Whole, Anemone Pulsatilla, Sodium Chloride, And Sus Scrofa Eye

N-21 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; Silicon Dioxide; Euphrasia Stricta; Ruta Graveolens Whole; Gelsemium Sempervirens Whole; Physostigma Venenosum Whole; Anemone Pulsatilla; Sodium Chloride; Sus Scrofa Eye.

Product ID58264-0219_1d774c26-378e-40c1-b237-28f2044c49cd
NDC58264-0219
Product TypeHuman Otc Drug
Proprietary NameN-21
Generic NameCalcium Fluoride, Silicon Dioxide, Euphrasia Stricta, Ruta Graveolens Whole, Gelsemium Sempervirens Whole, Physostigma Venenosum Whole, Anemone Pulsatilla, Sodium Chloride, And Sus Scrofa Eye
Dosage FormSolution
Route of AdministrationSUBLINGUAL
Marketing Start Date1990-01-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameDNA Labs, Inc.
Substance NameCALCIUM FLUORIDE; SILICON DIOXIDE; EUPHRASIA STRICTA; RUTA GRAVEOLENS WHOLE; GELSEMIUM SEMPERVIRENS WHOLE; PHYSOSTIGMA VENENOSUM WHOLE; ANEMONE PULSATILLA; SODIUM CHLORIDE; SUS SCROFA EYE
Active Ingredient Strength6 [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 58264-0219-1

29.57 mL in 1 BOTTLE, GLASS (58264-0219-1)
Marketing Start Date1990-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 58264-0219-1 [58264021901]

N-21 SOLUTION
Marketing CategoryUnapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date1990-01-01
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
CALCIUM FLUORIDE6 [hp_X]/mL

OpenFDA Data

SPL SET ID:89967941-c4ee-4598-a66d-8a93d69a4d65
Manufacturer
UNII
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