PreviDent - 0126-0288-02 - (Sodium Fluoride)

Alphabetical Index


Drug Information of PreviDent

Product NDC: 0126-0288
Proprietary Name: PreviDent
Non Proprietary Name: Sodium Fluoride
Active Ingredient(s): 11    mg/g & nbsp;   Sodium Fluoride
Administration Route(s): DENTAL
Dosage Form(s): GEL, DENTIFRICE
Coding System: National Drug Codes(NDC)

Labeler Information of PreviDent

Product NDC: 0126-0288
Labeler Name: Colgate Oral Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20120829

Package Information of PreviDent

Package NDC: 0126-0288-02
Package Description: 1 TUBE in 1 CARTON (0126-0288-02) > 56 g in 1 TUBE

NDC Information of PreviDent

NDC Code 0126-0288-02
Proprietary Name PreviDent
Package Description 1 TUBE in 1 CARTON (0126-0288-02) > 56 g in 1 TUBE
Product NDC 0126-0288
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sodium Fluoride
Dosage Form Name GEL, DENTIFRICE
Route Name DENTAL
Start Marketing Date 20120829
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Colgate Oral Pharmaceuticals, Inc.
Substance Name SODIUM FLUORIDE
Strength Number 11
Strength Unit mg/g
Pharmaceutical Classes

Complete Information of PreviDent


General Information