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LBEL EFFET PARFAIT - 13537-434-02 - (Octinoxate and Titanium Dioxide)

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Drug Information of LBEL EFFET PARFAIT

Product NDC: 13537-434
Proprietary Name: LBEL EFFET PARFAIT
Non Proprietary Name: Octinoxate and Titanium Dioxide
Active Ingredient(s): .07; .024    g/mL; g/mL & nbsp;   Octinoxate and Titanium Dioxide
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of LBEL EFFET PARFAIT

Product NDC: 13537-434
Labeler Name: Ventura Corporation LTD.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20120914

Package Information of LBEL EFFET PARFAIT

Package NDC: 13537-434-02
Package Description: 1 BOTTLE in 1 BOX (13537-434-02) > 1 mL in 1 BOTTLE (13537-434-01)

NDC Information of LBEL EFFET PARFAIT

NDC Code 13537-434-02
Proprietary Name LBEL EFFET PARFAIT
Package Description 1 BOTTLE in 1 BOX (13537-434-02) > 1 mL in 1 BOTTLE (13537-434-01)
Product NDC 13537-434
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Octinoxate and Titanium Dioxide
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20120914
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Ventura Corporation LTD.
Substance Name OCTINOXATE; TITANIUM DIOXIDE
Strength Number .07; .024
Strength Unit g/mL; g/mL
Pharmaceutical Classes

Complete Information of LBEL EFFET PARFAIT


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