"48951-3222-1" National Drug Code (NDC)

NDC Code	48951-3222-1
Package Description	10 AMPULE in 1 BOX (48951-3222-1) > 1 mL in 1 AMPULE
Product NDC	48951-3222
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Cutis 8 Special Order
Non-Proprietary Name	Cutis 8 Special Order
Dosage Form	LIQUID
Usage	ORAL
Start Marketing Date	20090901
Marketing Category Name	UNAPPROVED HOMEOPATHIC
Manufacturer	Uriel Pharmacy Inc.
Substance Name	SUS SCROFA SKIN
Strength	8
Strength Unit	[hp_X]/mL
Pharmacy Classes	Allergens [CS], Cell-mediated Immunity [PE], Cells, Epidermal [EXT], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Animal Skin Allergenic Extract [EPC]