Product NDC: | 64980-306 |
Proprietary Name: | Denta 5000 Plus |
Non Proprietary Name: | Sodium fluoride |
Active Ingredient(s): | 1.1 g/100g & nbsp; Sodium fluoride |
Administration Route(s): | ORAL |
Dosage Form(s): | GEL, DENTIFRICE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 64980-306 |
Labeler Name: | Rising Pharmaceuticals, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20120713 |
Package NDC: | 64980-306-50 |
Package Description: | 2 TUBE in 1 CARTON (64980-306-50) > 51 g in 1 TUBE |
NDC Code | 64980-306-50 |
Proprietary Name | Denta 5000 Plus |
Package Description | 2 TUBE in 1 CARTON (64980-306-50) > 51 g in 1 TUBE |
Product NDC | 64980-306 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Sodium fluoride |
Dosage Form Name | GEL, DENTIFRICE |
Route Name | ORAL |
Start Marketing Date | 20120713 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Rising Pharmaceuticals, Inc. |
Substance Name | SODIUM FLUORIDE |
Strength Number | 1.1 |
Strength Unit | g/100g |
Pharmaceutical Classes |