Home > National Drug Code (NDC) > EFFET PARFAIT

EFFET PARFAIT - 13537-023-08 - (Octinoxate and Titanium Dioxide)

Alphabetical Index


Drug Information of EFFET PARFAIT

Product NDC: 13537-023
Proprietary Name: EFFET PARFAIT
Non Proprietary Name: Octinoxate and Titanium Dioxide
Active Ingredient(s): .065; .016    mL/mL; mL/mL & nbsp;   Octinoxate and Titanium Dioxide
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of EFFET PARFAIT

Product NDC: 13537-023
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 EFFET PARFAIT

Package NDC: 13537-023-08
Package Description: 1 BOTTLE in 1 CARTON (13537-023-08) > 40.5 mL in 1 BOTTLE (13537-023-07)

NDC Information of EFFET PARFAIT

NDC Code 13537-023-08
Proprietary Name EFFET PARFAIT
Package Description 1 BOTTLE in 1 CARTON (13537-023-08) > 40.5 mL in 1 BOTTLE (13537-023-07)
Product NDC 13537-023
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Octinoxate and Titanium Dioxide
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20110810
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Ventura Corporation Ltd.
Substance Name OCTINOXATE; TITANIUM DIOXIDE
Strength Number .065; .016
Strength Unit mL/mL; mL/mL
Pharmaceutical Classes

Complete Information of EFFET PARFAIT


General Information