Home > National Drug Code (NDC) > Dr. Lewinn by Kinerase

Dr. Lewinn by Kinerase - 0187-1824-01 - (Octinoxate, Zinc Oxide)

Alphabetical Index


Drug Information of Dr. Lewinn by Kinerase

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)

Labeler Information of Dr. Lewinn by Kinerase

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 Information of Dr. Lewinn by Kinerase

Package NDC: 0187-1824-01
Package Description: 48 g in 1 TUBE (0187-1824-01)

NDC Information of Dr. Lewinn by Kinerase

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

Complete Information of Dr. Lewinn by Kinerase


General Information