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 |