| Product NDC: | 0187-1824 |
| Proprietary Name: | Dr. Lewinn by Kinerase |
| Non Proprietary Name: | Octinoxate, Zinc Oxide |
| Active Ingredient(s): | 2.88; 1.44 g/48g; g/48g & nbsp; Octinoxate, Zinc Oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0187-1824 |
| Labeler Name: | Valeant Pharmaceuticals North America LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20121205 |
| Package NDC: | 0187-1824-01 |
| Package Description: | 48 g in 1 TUBE (0187-1824-01) |
| NDC Code | 0187-1824-01 |
| Proprietary Name | Dr. Lewinn by Kinerase |
| Package Description | 48 g in 1 TUBE (0187-1824-01) |
| Product NDC | 0187-1824 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate, Zinc Oxide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20121205 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Valeant Pharmaceuticals North America LLC |
| Substance Name | OCTINOXATE; ZINC OXIDE |
| Strength Number | 2.88; 1.44 |
| Strength Unit | g/48g; g/48g |
| Pharmaceutical Classes |