Product NDC: | 42002-447 |
Proprietary Name: | Listerine Ultraclean Antiseptic |
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): | ORAL |
Dosage Form(s): | MOUTHWASH |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 42002-447 |
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: | 20120709 |
Package NDC: | 42002-447-73 |
Package Description: | 250 mL in 1 BOTTLE, PLASTIC (42002-447-73) |
NDC Code | 42002-447-73 |
Proprietary Name | Listerine Ultraclean Antiseptic |
Package Description | 250 mL in 1 BOTTLE, PLASTIC (42002-447-73) |
Product NDC | 42002-447 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Eucalyptol, Menthol, Methyl Salicylate, and Thymol |
Dosage Form Name | MOUTHWASH |
Route Name | ORAL |
Start Marketing Date | 20120709 |
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 |