Product NDC: | 63783-501 |
Proprietary Name: | NEUTRAMAXX 5000 TCP |
Non Proprietary Name: | SODIUM FLUORIDE |
Active Ingredient(s): | 1.1 g/112g & nbsp; SODIUM FLUORIDE |
Administration Route(s): | ORAL |
Dosage Form(s): | PASTE, DENTIFRICE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63783-501 |
Labeler Name: | Massco Dental A Division of Dunagin Pharmaceuticals |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | part355 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110801 |
Package NDC: | 63783-501-04 |
Package Description: | 112 g in 1 TUBE (63783-501-04) |
NDC Code | 63783-501-04 |
Proprietary Name | NEUTRAMAXX 5000 TCP |
Package Description | 112 g in 1 TUBE (63783-501-04) |
Product NDC | 63783-501 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | SODIUM FLUORIDE |
Dosage Form Name | PASTE, DENTIFRICE |
Route Name | ORAL |
Start Marketing Date | 20110801 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Massco Dental A Division of Dunagin Pharmaceuticals |
Substance Name | SODIUM FLUORIDE |
Strength Number | 1.1 |
Strength Unit | g/112g |
Pharmaceutical Classes |