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Listerine Whitening Restoring
Listerine Whitening Restoring - 42002-420-16 - (Sodium Fluoride)
Drug Information of Listerine Whitening Restoring
| Product NDC: | 42002-420 |
| Proprietary Name: | Listerine Whitening Restoring |
| Non Proprietary Name: | Sodium Fluoride |
| Active Ingredient(s): | .2 mg/mL & nbsp; Sodium Fluoride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | RINSE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Listerine Whitening Restoring
| Product NDC: | 42002-420 |
| 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: | 20120501 |
Package Information of Listerine Whitening Restoring
| Package NDC: | 42002-420-16 |
| Package Description: | 473 mL in 1 BOTTLE, PLASTIC (42002-420-16) |
NDC Information of Listerine Whitening Restoring
| NDC Code | 42002-420-16 |
| Proprietary Name | Listerine Whitening Restoring |
| Package Description | 473 mL in 1 BOTTLE, PLASTIC (42002-420-16) |
| Product NDC | 42002-420 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sodium Fluoride |
| Dosage Form Name | RINSE |
| Route Name | ORAL |
| Start Marketing Date | 20120501 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc. |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | .2 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
