Product NDC: | 53567-0101 |
Proprietary Name: | SuperSmile Professional |
Non Proprietary Name: | Fluoride |
Active Ingredient(s): | .76 g/100g & nbsp; Fluoride |
Administration Route(s): | DENTAL |
Dosage Form(s): | PASTE, DENTIFRICE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 53567-0101 |
Labeler Name: | ROBELL RESEARCH, INC. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part355 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110628 |
Package NDC: | 53567-0101-6 |
Package Description: | 227 g in 1 TUBE (53567-0101-6) |
NDC Code | 53567-0101-6 |
Proprietary Name | SuperSmile Professional |
Package Description | 227 g in 1 TUBE (53567-0101-6) |
Product NDC | 53567-0101 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Fluoride |
Dosage Form Name | PASTE, DENTIFRICE |
Route Name | DENTAL |
Start Marketing Date | 20110628 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | ROBELL RESEARCH, INC. |
Substance Name | SODIUM MONOFLUOROPHOSPHATE |
Strength Number | .76 |
Strength Unit | g/100g |
Pharmaceutical Classes |