"48951-2149-9" National Drug Code (NDC)

NDC Code	48951-2149-9
Package Description	240 mL in 1 BOTTLE, GLASS (48951-2149-9)
Product NDC	48951-2149
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Birch Juniper
Non-Proprietary Name	Birch Juniper
Dosage Form	LIQUID
Usage	ORAL
Start Marketing Date	20211103
Marketing Category Name	UNAPPROVED HOMEOPATHIC
Manufacturer	Uriel Pharmacy Inc
Substance Name	BETULA PENDULA BARK; JUNIPER BERRY
Strength	1; 1
Strength Unit	[hp_X]/mL; [hp_X]/mL
Pharmacy Classes	Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Food Additives [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS]