Product NDC: | 42002-443 |
Proprietary Name: | Listerine Total Care Zero |
Non Proprietary Name: | Sodium Fluoride |
Active Ingredient(s): | .221 g/mL & nbsp; Sodium Fluoride |
Administration Route(s): | ORAL |
Dosage Form(s): | MOUTHWASH |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 42002-443 |
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: | 20110501 |
Package NDC: | 42002-443-71 |
Package Description: | 1000 mL in 1 BOTTLE, PLASTIC (42002-443-71) |
NDC Code | 42002-443-71 |
Proprietary Name | Listerine Total Care Zero |
Package Description | 1000 mL in 1 BOTTLE, PLASTIC (42002-443-71) |
Product NDC | 42002-443 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Sodium Fluoride |
Dosage Form Name | MOUTHWASH |
Route Name | ORAL |
Start Marketing Date | 20110501 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc. |
Substance Name | SODIUM FLUORIDE |
Strength Number | .221 |
Strength Unit | g/mL |
Pharmaceutical Classes |