Product NDC: | 51009-116 |
Proprietary Name: | Cavity Protection |
Non Proprietary Name: | Sodium Monofluorophosphate |
Active Ingredient(s): | .0076 g/g & nbsp; Sodium Monofluorophosphate |
Administration Route(s): | DENTAL |
Dosage Form(s): | PASTE, DENTIFRICE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51009-116 |
Labeler Name: | Tom's of Maine, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part355 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110214 |
Package NDC: | 51009-116-55 |
Package Description: | 1 TUBE in 1 CARTON (51009-116-55) > 155.9 g in 1 TUBE |
NDC Code | 51009-116-55 |
Proprietary Name | Cavity Protection |
Package Description | 1 TUBE in 1 CARTON (51009-116-55) > 155.9 g in 1 TUBE |
Product NDC | 51009-116 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Sodium Monofluorophosphate |
Dosage Form Name | PASTE, DENTIFRICE |
Route Name | DENTAL |
Start Marketing Date | 20110214 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Tom's of Maine, Inc. |
Substance Name | SODIUM MONOFLUOROPHOSPHATE |
Strength Number | .0076 |
Strength Unit | g/g |
Pharmaceutical Classes |