Home
>
National Drug Code (NDC)
>
Cavity Protection
Cavity Protection - 51009-120-55 - (Sodium Monofluorophosphate)
Drug Information of Cavity Protection
| Product NDC: | 51009-120 |
| 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) |
Labeler Information of Cavity Protection
| Product NDC: | 51009-120 |
| 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 Information of Cavity Protection
| Package NDC: | 51009-120-55 |
| Package Description: | 1 TUBE in 1 CARTON (51009-120-55) > 155.9 g in 1 TUBE |
NDC Information of Cavity Protection
| NDC Code | 51009-120-55 |
| Proprietary Name | Cavity Protection |
| Package Description | 1 TUBE in 1 CARTON (51009-120-55) > 155.9 g in 1 TUBE |
| Product NDC | 51009-120 |
| 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 |
