Product NDC: | 42002-412 |
Proprietary Name: | Listerine Essential Care Tartar Control |
Non Proprietary Name: | Sodium Monofluorophosphate |
Active Ingredient(s): | 1.3 mg/g & nbsp; Sodium Monofluorophosphate |
Administration Route(s): | ORAL |
Dosage Form(s): | GEL, DENTIFRICE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 42002-412 |
Labeler Name: | Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part355 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120312 |
Package NDC: | 42002-412-09 |
Package Description: | 1 TUBE in 1 CARTON (42002-412-09) > 119 g in 1 TUBE |
NDC Code | 42002-412-09 |
Proprietary Name | Listerine Essential Care Tartar Control |
Package Description | 1 TUBE in 1 CARTON (42002-412-09) > 119 g in 1 TUBE |
Product NDC | 42002-412 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Sodium Monofluorophosphate |
Dosage Form Name | GEL, DENTIFRICE |
Route Name | ORAL |
Start Marketing Date | 20120312 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc. |
Substance Name | SODIUM MONOFLUOROPHOSPHATE |
Strength Number | 1.3 |
Strength Unit | mg/g |
Pharmaceutical Classes |