"48951-1352-1" National Drug Code (NDC)

NDC Code	48951-1352-1
Package Description	10 AMPULE in 1 BOX (48951-1352-1) / 1 mL in 1 AMPULE
Product NDC	48951-1352
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Arnica Betula A
Non-Proprietary Name	Arnica Betula A
Dosage Form	LIQUID
Usage	ORAL
Start Marketing Date	20090901
Marketing Category Name	UNAPPROVED HOMEOPATHIC
Manufacturer	Uriel Pharmacy Inc.
Substance Name	ARNICA MONTANA FLOWER; BETULA PENDULA LEAF; BETULA PUBESCENS BARK; BOS TAURUS BRAIN; BOS TAURUS CEREBELLUM; BOS TAURUS EYE; BOS TAURUS NERVE; BOS TAURUS PITUITARY GLAND; C12-17 ALKANE; FORMICA RUFA; HONEY; LEAD; SILICON DIOXIDE; SUS SCROFA THALAMUS
Strength	30; 3; 4; 17; 17; 17; 17; 17; 17; 30; 30; 30; 30; 17
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