"15821-501-90" National Drug Code (NDC)

NDC Code	15821-501-90
Package Description	90 CAPSULE, GELATIN COATED in 1 BOTTLE (15821-501-90)
Product NDC	15821-501
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Tozal
Non-Proprietary Name	Softgel
Dosage Form	CAPSULE, GELATIN COATED
Usage	ORAL
Start Marketing Date	20130601
Marketing Category Name	UNAPPROVED DRUG OTHER
Manufacturer	FOCUS Laboratories, Inc.
Substance Name	VITAMIN A PALMITATE; ASCORBIC ACID; CHOLECALCIFEROL; ALPHA-TOCOPHEROL; PYRIDOXINE HYDROCHLORIDE; FOLIC ACID; CYANOCOBALAMIN; ZINC PICOLINATE; COPPER; OMEGA-3 FATTY ACIDS; TAURINE; LUTEIN; ZEAXANTHIN
Strength	10000; 452; 1000; 200; 20; 1; 100; 40; 1.6; 600; 400; 15; 3
Strength Unit	[iU]/31; mg/31; [iU]/31; [iU]/31; mg/31; mg/31; ug/31; mg/31; mg/31; mg/31; mg/31; mg/31; mg/31
Pharmacy Classes	Vitamin A [Chemical/Ingredient],Vitamin A [EPC],Vitamin D [Chemical/Ingredient],Vitamin D [EPC],Vitamin B 12 [Chemical/Ingredient],Vitamin B12 [EPC],Copper Absorption Inhibitor [EPC],Decreased Copper Ion Absorption [PE],Copper [Chemical/Ingredient],Copper-containing Intrauterine Device [EPC],Decreased Embryonic Implantation [PE],Decreased Sperm Motility [PE],Inhibit Ovum Fertilization [PE],Fatty Acids, Omega-3 [Chemical/Ingredient],Omega-3 Fatty Acid [EPC]