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LISTERINE
LISTERINE - 42002-421-73 - (Sodium fluoride)
Drug Information of LISTERINE
| Product NDC: | 42002-421 |
| Proprietary Name: | LISTERINE |
| Non Proprietary Name: | Sodium fluoride |
| Active Ingredient(s): | 2.21 mg/10mL & nbsp; Sodium fluoride |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | MOUTHWASH |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LISTERINE
| Product NDC: | 42002-421 |
| 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: | 20091130 |
Package Information of LISTERINE
| Package NDC: | 42002-421-73 |
| Package Description: | 250 mL in 1 BOTTLE, PLASTIC (42002-421-73) |
NDC Information of LISTERINE
| NDC Code | 42002-421-73 |
| Proprietary Name | LISTERINE |
| Package Description | 250 mL in 1 BOTTLE, PLASTIC (42002-421-73) |
| Product NDC | 42002-421 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sodium fluoride |
| Dosage Form Name | MOUTHWASH |
| Route Name | DENTAL |
| Start Marketing Date | 20091130 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc. |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | 2.21 |
| Strength Unit | mg/10mL |
| Pharmaceutical Classes |
