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Plak Smacker
Plak Smacker - 55346-0719-1 - (Sodium Fluoride)
Drug Information of Plak Smacker
| Product NDC: | 55346-0719 |
| Proprietary Name: | Plak Smacker |
| Non Proprietary Name: | Sodium Fluoride |
| Active Ingredient(s): | .4 mg/g & nbsp; Sodium Fluoride |
| Administration Route(s): | DENTAL; ORAL |
| Dosage Form(s): | PASTE, DENTIFRICE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Plak Smacker
| Product NDC: | 55346-0719 |
| Labeler Name: | Dental Technologies, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20071231 |
Package Information of Plak Smacker
| Package NDC: | 55346-0719-1 |
| Package Description: | 24 g in 1 TUBE (55346-0719-1) |
NDC Information of Plak Smacker
| NDC Code | 55346-0719-1 |
| Proprietary Name | Plak Smacker |
| Package Description | 24 g in 1 TUBE (55346-0719-1) |
| Product NDC | 55346-0719 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sodium Fluoride |
| Dosage Form Name | PASTE, DENTIFRICE |
| Route Name | DENTAL; ORAL |
| Start Marketing Date | 20071231 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Dental Technologies, Inc |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | .4 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
