Product NDC: | 76357-106 |
Proprietary Name: | SmartMouth |
Non Proprietary Name: | Sodium Monofluorophosphate |
Active Ingredient(s): | 17 g/170g & nbsp; Sodium Monofluorophosphate |
Administration Route(s): | DENTAL |
Dosage Form(s): | PASTE, DENTIFRICE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 76357-106 |
Labeler Name: | Triumph Pharmaceuticals Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part355 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110617 |
Package NDC: | 76357-106-04 |
Package Description: | 170 g in 1 TUBE (76357-106-04) |
NDC Code | 76357-106-04 |
Proprietary Name | SmartMouth |
Package Description | 170 g in 1 TUBE (76357-106-04) |
Product NDC | 76357-106 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Sodium Monofluorophosphate |
Dosage Form Name | PASTE, DENTIFRICE |
Route Name | DENTAL |
Start Marketing Date | 20110617 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Triumph Pharmaceuticals Inc. |
Substance Name | SODIUM MONOFLUOROPHOSPHATE |
Strength Number | 17 |
Strength Unit | g/170g |
Pharmaceutical Classes |