| Product NDC: | 42002-411 |
| Proprietary Name: | Listerine Essential Care |
| Non Proprietary Name: | Sodium Monofluorophosphate |
| Active Ingredient(s): | 7.6 mg/g & nbsp; Sodium Monofluorophosphate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | GEL, DENTIFRICE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 42002-411 |
| 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: | 42002-411-09 |
| Package Description: | 1 TUBE in 1 CARTON (42002-411-09) > 119 g in 1 TUBE |
| NDC Code | 42002-411-09 |
| Proprietary Name | Listerine Essential Care |
| Package Description | 1 TUBE in 1 CARTON (42002-411-09) > 119 g in 1 TUBE |
| Product NDC | 42002-411 |
| 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 | 7.6 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |