Product NDC: | 51523-105 |
Proprietary Name: | FACE IT AQUA TINTED BB SPF 20 PA 01 |
Non Proprietary Name: | TITANIUM DIOXIDE, OCTINOXATE |
Active Ingredient(s): | 5; 5.8 mL/100mL; mL/100mL & nbsp; TITANIUM DIOXIDE, OCTINOXATE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51523-105 |
Labeler Name: | THEFACESHOP CO., LTD |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110823 |
Package NDC: | 51523-105-02 |
Package Description: | 1 CONTAINER in 1 BOX (51523-105-02) > 40 mL in 1 CONTAINER (51523-105-01) |
NDC Code | 51523-105-02 |
Proprietary Name | FACE IT AQUA TINTED BB SPF 20 PA 01 |
Package Description | 1 CONTAINER in 1 BOX (51523-105-02) > 40 mL in 1 CONTAINER (51523-105-01) |
Product NDC | 51523-105 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | TITANIUM DIOXIDE, OCTINOXATE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20110823 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | THEFACESHOP CO., LTD |
Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
Strength Number | 5; 5.8 |
Strength Unit | mL/100mL; mL/100mL |
Pharmaceutical Classes |