| Product NDC: | 51523-106 |
| Proprietary Name: | FACE IT AQUA TINTED BB SPF 20 PA 02 |
| 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: | 51523-106 |
| 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: | 51523-106-02 |
| Package Description: | 1 CONTAINER in 1 BOX (51523-106-02) > 40 mL in 1 CONTAINER (51523-106-01) |
| NDC Code | 51523-106-02 |
| Proprietary Name | FACE IT AQUA TINTED BB SPF 20 PA 02 |
| Package Description | 1 CONTAINER in 1 BOX (51523-106-02) > 40 mL in 1 CONTAINER (51523-106-01) |
| Product NDC | 51523-106 |
| 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 |