| Product NDC: | 57660-000 |
| Proprietary Name: | Fresh Mint Plaque HD Professional Plaque Identifying |
| Non Proprietary Name: | SODIUM FLUORIDE |
| Active Ingredient(s): | .14 g/100g & nbsp; SODIUM FLUORIDE |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | PASTE, DENTIFRICE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 57660-000 |
| Labeler Name: | TJA Health LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130610 |
| Package NDC: | 57660-000-02 |
| Package Description: | 1 TUBE in 1 PACKAGE (57660-000-02) > 21 g in 1 TUBE |
| NDC Code | 57660-000-02 |
| Proprietary Name | Fresh Mint Plaque HD Professional Plaque Identifying |
| Package Description | 1 TUBE in 1 PACKAGE (57660-000-02) > 21 g in 1 TUBE |
| Product NDC | 57660-000 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SODIUM FLUORIDE |
| Dosage Form Name | PASTE, DENTIFRICE |
| Route Name | DENTAL |
| Start Marketing Date | 20130610 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | TJA Health LLC |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | .14 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |