| 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 |