| 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 |