LBEL - 13537-240-02 - (OCTINOXATE and OXYBENZONE)

Alphabetical Index


Drug Information of LBEL

Product NDC: 13537-240
Proprietary Name: LBEL
Non Proprietary Name: OCTINOXATE and OXYBENZONE
Active Ingredient(s): .075; .02    g/g; g/g & nbsp;   OCTINOXATE and OXYBENZONE
Administration Route(s): TOPICAL
Dosage Form(s): POWDER
Coding System: National Drug Codes(NDC)

Labeler Information of LBEL

Product NDC: 13537-240
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: 20100816

Package Information of LBEL

Package NDC: 13537-240-02
Package Description: 1 CASE in 1 BOX (13537-240-02) > 8 g in 1 CASE (13537-240-01)

NDC Information of LBEL

NDC Code 13537-240-02
Proprietary Name LBEL
Package Description 1 CASE in 1 BOX (13537-240-02) > 8 g in 1 CASE (13537-240-01)
Product NDC 13537-240
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTINOXATE and OXYBENZONE
Dosage Form Name POWDER
Route Name TOPICAL
Start Marketing Date 20100816
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Ventura Corporation (San Juan, P.R.)
Substance Name OCTINOXATE; OXYBENZONE
Strength Number .075; .02
Strength Unit g/g; g/g
Pharmaceutical Classes

Complete Information of LBEL


General Information