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Listerine
Listerine - 42002-427-08 - (Sodium Fluoride)
Drug Information of Listerine
| Product NDC: | 42002-427 |
| Proprietary Name: | Listerine |
| Non Proprietary Name: | Sodium Fluoride |
| Active Ingredient(s): | .0221 g/mL & nbsp; Sodium Fluoride |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | MOUTHWASH |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Listerine
| Product NDC: | 42002-427 |
| 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: | 20100701 |
Package Information of Listerine
| Package NDC: | 42002-427-08 |
| Package Description: | 236 mL in 1 BOTTLE, PLASTIC (42002-427-08) |
NDC Information of Listerine
| NDC Code | 42002-427-08 |
| Proprietary Name | Listerine |
| Package Description | 236 mL in 1 BOTTLE, PLASTIC (42002-427-08) |
| Product NDC | 42002-427 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sodium Fluoride |
| Dosage Form Name | MOUTHWASH |
| Route Name | DENTAL |
| Start Marketing Date | 20100701 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc. |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | .0221 |
| Strength Unit | g/mL |
| Pharmaceutical Classes |
