Home NDC 58264-0214-1 N-16
Product NDC 58264-0214
Requested package NDC 58264-0214-1
11-digit product format 582640214
Labeler code 58264
Product ID 58264-0214_2b539c7f-71e3-1665-e063-6294a90ab35a
Type HUMAN OTC DRUG
Nonproprietary name mgo energizer
Dosage form SOLUTION
Route SUBLINGUAL
Labeler DNA Labs, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1990-01-01
Substance ASCORBIC ACID; BEEF HEART; BOS TAURUS ADRENAL GLAND; BOS TAURUS PITUITARY GLAND, POSTERIOR; BOS TAURUS THYMUS; CALCIUM FLUORIDE; CALCIUM SULFATE ANHYDROUS; DIBASIC POTASSIUM PHOSPHATE; FERROSOFERRIC PHOSPHATE; GLYCINE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; MAMMAL LIVER; PORK BRAIN; POTASSIUM CHLORIDE; POTASSIUM SULFATE; PYRIDOXINE HYDROCHLORIDE; SILICON DIOXIDE; SODIUM CHLORIDE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SODIUM SULFATE; SUS SCROFA DUODENUM; SUS SCROFA LUNG; SUS SCROFA PANCREAS; SUS SCROFA SPLEEN; THYROID, UNSPECIFIED; TRIBASIC CALCIUM PHOSPHATE; TRIPE
Active strength 3; 200; 200; 200; 200; 30; 30; 30; 30; 4; 30; 200; 200; 30; 30; 3; 30; 30; 30; 30; 200; 200; 200; 200; 200; 30; 200 [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
Pharmacologic classes Analogs/Derivatives [Chemical/Ingredient], Ascorbic Acid [CS], Blood Coagulation Factor [EPC], Calcium [CS], Calculi Dissolution Agent [EPC], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Potassium Compounds [CS], Potassium Compounds [CS], Potassium Salt [EPC], Potassium Salt [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE], Vitamin B 6 [Chemical/Ingredient], Vitamin B6 Analog [EPC], Vitamin C [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 5 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2022-04-09 23:13 UTC · source 2022-04-08 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 bd6a592717d7…303034d00443…2021-12-27 23:28 UTC · source 2021-12-27 8dfbde2a14a4…c9ff85d89658…2020-12-18 03:04 UTC · source 2020-12-17 e2bbac7714bc…27bdfed8d636…2020-06-10 20:45 UTC · source 2020-06-10 9bebd1f3094a…5416666fcb17…
Additional Listing Data#
Finished product Yes
Brand name base N-16
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BOS TAURUS ADRENAL GLAND 3 [hp_X]/mL BOS TAURUS THYMUS 200 [hp_X]/mL SUS SCROFA SPLEEN 200 [hp_X]/mL TRIPE 200 [hp_X]/mL BOS TAURUS PITUITARY GLAND, POSTERIOR 200 [hp_X]/mL MAMMAL LIVER 30 [hp_X]/mL SUS SCROFA LUNG 30 [hp_X]/mL BEEF HEART 30 [hp_X]/mL PORK BRAIN 30 [hp_X]/mL SUS SCROFA DUODENUM 4 [hp_X]/mL SUS SCROFA PANCREAS 30 [hp_X]/mL THYROID, UNSPECIFIED 200 [hp_X]/mL PYRIDOXINE HYDROCHLORIDE 200 [hp_X]/mL ASCORBIC ACID 30 [hp_X]/mL GLYCINE 30 [hp_X]/mL CALCIUM FLUORIDE 3 [hp_X]/mL TRIBASIC CALCIUM PHOSPHATE 30 [hp_X]/mL CALCIUM SULFATE ANHYDROUS 30 [hp_X]/mL FERROSOFERRIC PHOSPHATE 30 [hp_X]/mL POTASSIUM CHLORIDE 30 [hp_X]/mL DIBASIC POTASSIUM PHOSPHATE 200 [hp_X]/mL POTASSIUM SULFATE 200 [hp_X]/mL MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 200 [hp_X]/mL SODIUM CHLORIDE 200 [hp_X]/mL SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE 200 [hp_X]/mL SODIUM SULFATE 30 [hp_X]/mL SILICON DIOXIDE 200 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 2 · 26 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 58264-0214-1 N-16 29.57 mL in 1 BOTTLE, GLASS SOLUTION 29.57 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 58264-0214 N-16 (MGO ENERGIZER) SOLUTION [DNA LABS, INC.] 4 Current NDC, Legacy NDC, 1 package rows 20250112_8292b900-86c1-47ea-81da-b587439c7664.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 58264-0214-1 58264021401 29.57 mL in 1 BOTTLE, GLASS (58264-0214-1) 29.57 ml 1990-01-01 0000-00-00 No No Current