PreviDent - 0126-0075-92 - (Sodium fluoride)

Alphabetical Index


Drug Information of PreviDent

Product NDC: 0126-0075
Proprietary Name: PreviDent
Non Proprietary Name: Sodium fluoride
Active Ingredient(s): 13.4    mg/mL & nbsp;   Sodium fluoride
Administration Route(s): DENTAL
Dosage Form(s): GEL, DENTIFRICE
Coding System: National Drug Codes(NDC)

Labeler Information of PreviDent

Product NDC: 0126-0075
Labeler Name: Colgate-Palmolive Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20090706

Package Information of PreviDent

Package NDC: 0126-0075-92
Package Description: 100 mL in 1 BOTTLE (0126-0075-92)

NDC Information of PreviDent

NDC Code 0126-0075-92
Proprietary Name PreviDent
Package Description 100 mL in 1 BOTTLE (0126-0075-92)
Product NDC 0126-0075
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sodium fluoride
Dosage Form Name GEL, DENTIFRICE
Route Name DENTAL
Start Marketing Date 20090706
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Colgate-Palmolive Company
Substance Name SODIUM FLUORIDE
Strength Number 13.4
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of PreviDent


General Information