LBEL - 13537-031-02 - (Octinoxate, Octisalate, and Oxybenzone)

Alphabetical Index


Drug Information of LBEL

Product NDC: 13537-031
Proprietary Name: LBEL
Non Proprietary Name: Octinoxate, Octisalate, and Oxybenzone
Active Ingredient(s): .075; .04; .04    g/mL; g/mL; g/mL & nbsp;   Octinoxate, Octisalate, and Oxybenzone
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of LBEL

Product NDC: 13537-031
Labeler Name: Ventura Corporation Ltd. (San Juan, P.R)
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110829

Package Information of LBEL

Package NDC: 13537-031-02
Package Description: 1 TUBE in 1 BOX (13537-031-02) > 50 mL in 1 TUBE (13537-031-01)

NDC Information of LBEL

NDC Code 13537-031-02
Proprietary Name LBEL
Package Description 1 TUBE in 1 BOX (13537-031-02) > 50 mL in 1 TUBE (13537-031-01)
Product NDC 13537-031
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Octinoxate, Octisalate, and Oxybenzone
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20110829
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Ventura Corporation Ltd. (San Juan, P.R)
Substance Name OCTINOXATE; OCTISALATE; OXYBENZONE
Strength Number .075; .04; .04
Strength Unit g/mL; g/mL; g/mL
Pharmaceutical Classes

Complete Information of LBEL


General Information