"0126-0022-12" National Drug Code (NDC)

NDC Code	0126-0022-12
Package Description	3.5 mL in 1 PACKET (0126-0022-12)
Product NDC	0126-0022
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Prevident 5000 Enamel Protect
Non-Proprietary Name	Sodium Fluoride And Potassium Nitrate
Dosage Form	GEL, DENTIFRICE
Usage	DENTAL
Start Marketing Date	20110330
Marketing Category Name	UNAPPROVED DRUG OTHER
Manufacturer	Colgate Oral Pharmaceuticals, Inc.
Substance Name	SODIUM FLUORIDE; POTASSIUM NITRATE
Strength	5.8; 57.5
Strength Unit	mg/mL; mg/mL