Product NDC: | 14783-010 |
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) |
Product NDC: | 14783-010 |
Labeler Name: | Ventura International LTD. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20120914 |
Package NDC: | 14783-010-02 |
Package Description: | 1 BOTTLE in 1 BOX (14783-010-02) > 1 mL in 1 BOTTLE (14783-010-01) |
NDC Code | 14783-010-02 |
Proprietary Name | LBEL EFFET PARFAIT |
Package Description | 1 BOTTLE in 1 BOX (14783-010-02) > 1 mL in 1 BOTTLE (14783-010-01) |
Product NDC | 14783-010 |
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 International LTD. |
Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
Strength Number | .07; .024 |
Strength Unit | g/mL; g/mL |
Pharmaceutical Classes |