| Product NDC: | 55526-0003 |
| Proprietary Name: | NAVI Mate Silver |
| Non Proprietary Name: | Sodium Monofluorophosphate Silicon Dioxide |
| Active Ingredient(s): | 21.36; .552 g/120g; g/120g & nbsp; Sodium Monofluorophosphate Silicon Dioxide |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | PASTE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 55526-0003 |
| Labeler Name: | EQ Maxon Corp. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130401 |
| Package NDC: | 55526-0003-1 |
| Package Description: | 120 g in 1 TUBE (55526-0003-1) |
| NDC Code | 55526-0003-1 |
| Proprietary Name | NAVI Mate Silver |
| Package Description | 120 g in 1 TUBE (55526-0003-1) |
| Product NDC | 55526-0003 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sodium Monofluorophosphate Silicon Dioxide |
| Dosage Form Name | PASTE |
| Route Name | DENTAL |
| Start Marketing Date | 20130401 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | EQ Maxon Corp. |
| Substance Name | SILICON DIOXIDE; SODIUM MONOFLUOROPHOSPHATE |
| Strength Number | 21.36; .552 |
| Strength Unit | g/120g; g/120g |
| Pharmaceutical Classes |