"48951-5122-1" National Drug Code (NDC)

NDC Code	48951-5122-1
Package Description	10 AMPULE in 1 BOX (48951-5122-1) > 1 mL in 1 AMPULE
Product NDC	48951-5122
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Helleborus Comp. A
Non-Proprietary Name	Helleborus Comp. A
Dosage Form	LIQUID
Usage	ORAL
Start Marketing Date	20210311
Marketing Category Name	UNAPPROVED HOMEOPATHIC
Manufacturer	Uriel Pharmacy Inc.
Substance Name	ANTIMONY; ARSENIC TRIOXIDE; FORMICA RUFA; HELLEBORUS NIGER ROOT; LEAD MONOSILICATE; PHOSPHORUS; SILVER
Strength	6; 17; 6; 3; 20; 12; 8
Strength Unit	[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL