Product NDC: | 53329-083 |
Proprietary Name: | SparkleFresh |
Non Proprietary Name: | Sodium Monofluorophosphate |
Active Ingredient(s): | 7.6 mg/g & nbsp; Sodium Monofluorophosphate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | PASTE, DENTIFRICE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 53329-083 |
Labeler Name: | Medline Industries, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part355 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20070101 |
Package NDC: | 53329-083-21 |
Package Description: | 42.5 g in 1 TUBE (53329-083-21) |
NDC Code | 53329-083-21 |
Proprietary Name | SparkleFresh |
Package Description | 42.5 g in 1 TUBE (53329-083-21) |
Product NDC | 53329-083 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Sodium Monofluorophosphate |
Dosage Form Name | PASTE, DENTIFRICE |
Route Name | TOPICAL |
Start Marketing Date | 20070101 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Medline Industries, Inc. |
Substance Name | SODIUM MONOFLUOROPHOSPHATE |
Strength Number | 7.6 |
Strength Unit | mg/g |
Pharmaceutical Classes |