ESIKA - 13537-327-02 - (OCTINOXATE)

Alphabetical Index


Drug Information of ESIKA

Product NDC: 13537-327
Proprietary Name: ESIKA
Non Proprietary Name: OCTINOXATE
Active Ingredient(s): .06    g/g & nbsp;   OCTINOXATE
Administration Route(s): TOPICAL
Dosage Form(s): POWDER
Coding System: National Drug Codes(NDC)

Labeler Information of ESIKA

Product NDC: 13537-327
Labeler Name: Ventura Corporation (San Juan, P.R)
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110517

Package Information of ESIKA

Package NDC: 13537-327-02
Package Description: 1 JAR in 1 BOX (13537-327-02) > 30 g in 1 JAR (13537-327-01)

NDC Information of ESIKA

NDC Code 13537-327-02
Proprietary Name ESIKA
Package Description 1 JAR in 1 BOX (13537-327-02) > 30 g in 1 JAR (13537-327-01)
Product NDC 13537-327
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTINOXATE
Dosage Form Name POWDER
Route Name TOPICAL
Start Marketing Date 20110517
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Ventura Corporation (San Juan, P.R)
Substance Name OCTINOXATE
Strength Number .06
Strength Unit g/g
Pharmaceutical Classes

Complete Information of ESIKA


General Information