ControlRx - 48878-3100-2 - (sodium fluoride)

Alphabetical Index


Drug Information of ControlRx

Product NDC: 48878-3100
Proprietary Name: ControlRx
Non Proprietary Name: sodium fluoride
Active Ingredient(s): 11    mg/g & nbsp;   sodium fluoride
Administration Route(s): ORAL
Dosage Form(s): PASTE, DENTIFRICE
Coding System: National Drug Codes(NDC)

Labeler Information of ControlRx

Product NDC: 48878-3100
Labeler Name: 3M ESPE Dental Products
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20050101

Package Information of ControlRx

Package NDC: 48878-3100-2
Package Description: 2 TUBE in 1 BOX (48878-3100-2) > 57 g in 1 TUBE

NDC Information of ControlRx

NDC Code 48878-3100-2
Proprietary Name ControlRx
Package Description 2 TUBE in 1 BOX (48878-3100-2) > 57 g in 1 TUBE
Product NDC 48878-3100
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name sodium fluoride
Dosage Form Name PASTE, DENTIFRICE
Route Name ORAL
Start Marketing Date 20050101
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name 3M ESPE Dental Products
Substance Name SODIUM FLUORIDE
Strength Number 11
Strength Unit mg/g
Pharmaceutical Classes

Complete Information of ControlRx


General Information