LBEL - 13537-019-02 - (OCTINOXATE and OXYBENZONE)

Alphabetical Index


Drug Information of LBEL

Product NDC: 13537-019
Proprietary Name: LBEL
Non Proprietary Name: OCTINOXATE and OXYBENZONE
Active Ingredient(s): .071; .016    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 LBEL

Product NDC: 13537-019
Labeler Name: Ventura Corporation Ltd.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110810

Package Information of LBEL

Package NDC: 13537-019-02
Package Description: 12 TUBE in 1 CARTON (13537-019-02) > 4 g in 1 TUBE (13537-019-01)

NDC Information of LBEL

NDC Code 13537-019-02
Proprietary Name LBEL
Package Description 12 TUBE in 1 CARTON (13537-019-02) > 4 g in 1 TUBE (13537-019-01)
Product NDC 13537-019
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTINOXATE and OXYBENZONE
Dosage Form Name LIPSTICK
Route Name TOPICAL
Start Marketing Date 20110810
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Ventura Corporation Ltd.
Substance Name OCTINOXATE; OXYBENZONE
Strength Number .071; .016
Strength Unit g/g; g/g
Pharmaceutical Classes

Complete Information of LBEL


General Information