Product NDC: | 64893-001 |
Proprietary Name: | Binaca Anticavity Flouride Peppermint |
Non Proprietary Name: | SODIUM MONOFLUOROPHOSPHATE |
Active Ingredient(s): | .76 g/100g & nbsp; SODIUM MONOFLUOROPHOSPHATE |
Administration Route(s): | DENTAL |
Dosage Form(s): | PASTE, DENTIFRICE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 64893-001 |
Labeler Name: | Dr. Fresh, Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part355 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100504 |
Package NDC: | 64893-001-42 |
Package Description: | 1 TUBE in 1 BOX (64893-001-42) > 119 g in 1 TUBE |
NDC Code | 64893-001-42 |
Proprietary Name | Binaca Anticavity Flouride Peppermint |
Package Description | 1 TUBE in 1 BOX (64893-001-42) > 119 g in 1 TUBE |
Product NDC | 64893-001 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | SODIUM MONOFLUOROPHOSPHATE |
Dosage Form Name | PASTE, DENTIFRICE |
Route Name | DENTAL |
Start Marketing Date | 20100504 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Dr. Fresh, Inc |
Substance Name | SODIUM MONOFLUOROPHOSPHATE |
Strength Number | .76 |
Strength Unit | g/100g |
Pharmaceutical Classes |