"48951-8372-3" National Drug Code (NDC)

NDC Code	48951-8372-3
Package Description	60 mL in 1 BOTTLE, DROPPER (48951-8372-3)
Product NDC	48951-8372
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Reynoutria Lyme
Non-Proprietary Name	Reynoutria Lyme
Dosage Form	LIQUID
Usage	ORAL
Start Marketing Date	20210312
Marketing Category Name	UNAPPROVED HOMEOPATHIC
Manufacturer	Uriel Pharmacy Inc.
Substance Name	APIS MELLIFERA; ASTRAGALUS CHINENSIS SEED; ASTRAGALUS PROPINQUUS ROOT; COPPER; DIPSACUS FULLONUM WHOLE; GOLD; HELLEBORUS NIGER ROOT; REYNOUTRIA JAPONICA LEAF; SILICON DIOXIDE; SILVER
Strength	21; 30; 6; 17; 4; 30; 4; 3; 17; 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
Pharmacy Classes	Allergens [CS], Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Inhibit Ovum Fertilization [PE], Standardized Chemical Allergen [EPC], Standardized Insect Venom Allergenic Extract [EPC]