"57520-0957-1" National Drug Code (NDC)

NDC Code	57520-0957-1
Package Description	30 mL in 1 BOTTLE, DROPPER (57520-0957-1)
Product NDC	57520-0957
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Psoriaforce
Non-Proprietary Name	Baptisia Tinctoria, Berberis Vulgaris, Echinacea, Glycyrrhiza Glabra, Hydrastis Canadensis, Lappa Major, Phytolacca Decandra, Rhamnus Frangula Lappa Major, Phytolacca Decandra, Rhamnus Frangula, Rhamnus Purshiana, Trifolium Pratense, Xanthoxylum Fraxineum, Arsenicum Iodatum, Calcarea Carbonica, Clematis Erecta, Graphites,
Dosage Form	LIQUID
Usage	ORAL
Start Marketing Date	20111114
End Marketing Date	20161205
Marketing Category Name	UNAPPROVED HOMEOPATHIC
Manufacturer	Apotheca Company
Substance Name	BAPTISIA TINCTORIA ROOT; BERBERIS VULGARIS ROOT BARK; ECHINACEA, UNSPECIFIED; GLYCYRRHIZA GLABRA; GOLDENSEAL; ARCTIUM LAPPA ROOT; PHYTOLACCA AMERICANA ROOT; FRANGULA ALNUS BARK; FRANGULA PURSHIANA BARK; TRIFOLIUM PRATENSE FLOWER; ZANTHOXYLUM AMERICANUM BARK; ARSENIC TRIIODIDE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; CLEMATIS RECTA FLOWERING TOP; GRAPHITE; POTASSIUM CHLORIDE; POTASSIUM SULFATE; DAPHNE MEZEREUM BARK; KEROSENE; SEPIA OFFICINALIS JUICE
Strength	3; 3; 3; 3; 3; 3; 3; 3; 3; 3; 3; 12; 12; 12; 12; 12; 12; 12; 12; 12
Strength Unit	[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