Product NDC: | 55526-0002 |
Proprietary Name: | NAVI Mate Gold |
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: | 55526-0002 |
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: | 55526-0002-1 |
Package Description: | 120 g in 1 TUBE (55526-0002-1) |
NDC Code | 55526-0002-1 |
Proprietary Name | NAVI Mate Gold |
Package Description | 120 g in 1 TUBE (55526-0002-1) |
Product NDC | 55526-0002 |
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 |