Product NDC: | 41442-123 |
Proprietary Name: | Complexion Brightener SPF20 |
Non Proprietary Name: | Titanium dioxide and Zinc oxide |
Active Ingredient(s): | .84; 2.1 mL/30mL; mL/30mL & nbsp; Titanium dioxide and Zinc oxide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 41442-123 |
Labeler Name: | Omorovicza Kozmetikai Kft. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110301 |
Package NDC: | 41442-123-02 |
Package Description: | 50 mL in 1 BOTTLE, PUMP (41442-123-02) |
NDC Code | 41442-123-02 |
Proprietary Name | Complexion Brightener SPF20 |
Package Description | 50 mL in 1 BOTTLE, PUMP (41442-123-02) |
Product NDC | 41442-123 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Titanium dioxide and Zinc oxide |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20110301 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Omorovicza Kozmetikai Kft. |
Substance Name | TITANIUM DIOXIDE; ZINC OXIDE |
Strength Number | .84; 2.1 |
Strength Unit | mL/30mL; mL/30mL |
Pharmaceutical Classes |