NDC 58264-0214

N-16

Mgo Energizer

N-16 is a Sublingual Solution in the Human Otc Drug category. It is labeled and distributed by Dna Labs, Inc.. The primary component is Bos Taurus Adrenal Gland; Bos Taurus Thymus; Sus Scrofa Spleen; Tripe; Bos Taurus Pituitary Gland, Posterior; Mammal Liver; Sus Scrofa Lung; Beef Heart; Pork Brain; Sus Scrofa Duodenum; Sus Scrofa Pancreas; Thyroid, Unspecified; Pyridoxine Hydrochloride; Ascorbic Acid; Glycine; Calcium Fluoride; Tribasic Calcium Phosphate; Calcium Sulfate Anhydrous; Ferrosoferric Phosphate; Potassium Chloride; Dibasic Potassium Phosphate; Potassium Sulfate; Magnesium Phosphate, Dibasic Trihydrate; Sodium Chloride; Sodium Phosphate, Dibasic, Heptahydrate; Sodium Sulfate; Silicon Dioxide.

Product ID58264-0214_a06ded86-26dc-4fb6-a864-b987f52f4de1
NDC58264-0214
Product TypeHuman Otc Drug
Proprietary NameN-16
Generic NameMgo Energizer
Dosage FormSolution
Route of AdministrationSUBLINGUAL
Marketing Start Date1990-01-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameDNA Labs, Inc.
Substance NameBOS TAURUS ADRENAL GLAND; BOS TAURUS THYMUS; SUS SCROFA SPLEEN; TRIPE; BOS TAURUS PITUITARY GLAND, POSTERIOR; MAMMAL LIVER; SUS SCROFA LUNG; BEEF HEART; PORK BRAIN; SUS SCROFA DUODENUM; SUS SCROFA PANCREAS; THYROID, UNSPECIFIED; PYRIDOXINE HYDROCHLORIDE; ASCORBIC ACID; GLYCINE; CALCIUM FLUORIDE; TRIBASIC CALCIUM PHOSPHATE; CALCIUM SULFATE ANHYDROUS; FERROSOFERRIC PHOSPHATE; POTASSIUM CHLORIDE; DIBASIC POTASSIUM PHOSPHATE; POTASSIUM SULFATE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; SODIUM CHLORIDE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SODIUM SULFATE; SILICON DIOXIDE
Active Ingredient Strength200 [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; [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; [hp_X]/mL
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 58264-0214-1

29.57 mL in 1 BOTTLE, GLASS (58264-0214-1)
Marketing Start Date1990-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 58264-0214-1 [58264021401]

N-16 SOLUTION
Marketing CategoryUNAPPROVED HOMEOPATHIC
Product TypeHUMAN OTC DRUG
Marketing Start Date1990-01-01
Inactivation Date2020-01-31

Drug Details


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