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Soft Mint Listerine
Soft Mint Listerine - 42002-404-71 - (Eucalyptol, Menthol, Methyl Salicylate and Thymol)
Drug Information of Soft Mint Listerine
| Product NDC: | 42002-404 |
| Proprietary Name: | Soft Mint Listerine |
| Non Proprietary Name: | Eucalyptol, Menthol, Methyl Salicylate and Thymol |
| Active Ingredient(s): | .92; .42; .6; .64 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; Eucalyptol, Menthol, Methyl Salicylate and Thymol |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | MOUTHWASH |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Soft Mint Listerine
| Product NDC: | 42002-404 |
| Labeler Name: | Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part356 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100205 |
Package Information of Soft Mint Listerine
| Package NDC: | 42002-404-71 |
| Package Description: | 1000 mL in 1 BOTTLE, PLASTIC (42002-404-71) |
NDC Information of Soft Mint Listerine
| NDC Code | 42002-404-71 |
| Proprietary Name | Soft Mint Listerine |
| Package Description | 1000 mL in 1 BOTTLE, PLASTIC (42002-404-71) |
| Product NDC | 42002-404 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Eucalyptol, Menthol, Methyl Salicylate and Thymol |
| Dosage Form Name | MOUTHWASH |
| Route Name | DENTAL |
| Start Marketing Date | 20100205 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc. |
| Substance Name | EUCALYPTOL; MENTHOL; METHYL SALICYLATE; THYMOL |
| Strength Number | .92; .42; .6; .64 |
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |
