ESIKA - 13537-050-02 - (Octinoxate and Oxybenzone)

Alphabetical Index


Drug Information of ESIKA

Product NDC: 13537-050
Proprietary Name: ESIKA
Non Proprietary Name: Octinoxate and Oxybenzone
Active Ingredient(s): .065; .0182    g/g; g/g & nbsp;   Octinoxate and Oxybenzone
Administration Route(s): TOPICAL
Dosage Form(s): LIPSTICK
Coding System: National Drug Codes(NDC)

Labeler Information of ESIKA

Product NDC: 13537-050
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: 20110923

Package Information of ESIKA

Package NDC: 13537-050-02
Package Description: 1 TUBE in 1 BOX (13537-050-02) > 4 g in 1 TUBE (13537-050-01)

NDC Information of ESIKA

NDC Code 13537-050-02
Proprietary Name ESIKA
Package Description 1 TUBE in 1 BOX (13537-050-02) > 4 g in 1 TUBE (13537-050-01)
Product NDC 13537-050
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Octinoxate and Oxybenzone
Dosage Form Name LIPSTICK
Route Name TOPICAL
Start Marketing Date 20110923
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Ventura Corporation (San Juan, P.R)
Substance Name OCTINOXATE; OXYBENZONE
Strength Number .065; .0182
Strength Unit g/g; g/g
Pharmaceutical Classes

Complete Information of ESIKA


General Information