"0496-0708-03" National Drug Code (NDC)

NDC Code	0496-0708-03
Package Description	57 g in 1 TUBE (0496-0708-03)
Product NDC	0496-0708
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Pramosone E
Non-Proprietary Name	Hydrocortisone Acetate And Pramoxine Hydrochloride
Dosage Form	CREAM
Usage	TOPICAL
Start Marketing Date	20100205
End Marketing Date	20170131
Marketing Category Name	UNAPPROVED DRUG OTHER
Manufacturer	Ferndale Laboratories, Inc.
Substance Name	HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE
Strength	25; 10
Strength Unit	mg/g; mg/g
Pharmacy Classes	Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]