| Product NDC: | 68570-812 |
| Proprietary Name: | shu uemura face architect |
| Non Proprietary Name: | Octinoxate Zinc Oxide |
| Active Ingredient(s): | .8; .48 g/14g; g/14g & nbsp; Octinoxate Zinc Oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 68570-812 |
| Labeler Name: | Cosmelor Ltd |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100601 |
| Package NDC: | 68570-812-01 |
| Package Description: | 1 CONTAINER in 1 CARTON (68570-812-01) > 14 g in 1 CONTAINER |
| NDC Code | 68570-812-01 |
| Proprietary Name | shu uemura face architect |
| Package Description | 1 CONTAINER in 1 CARTON (68570-812-01) > 14 g in 1 CONTAINER |
| Product NDC | 68570-812 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate Zinc Oxide |
| Dosage Form Name | POWDER |
| Route Name | TOPICAL |
| Start Marketing Date | 20100601 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Cosmelor Ltd |
| Substance Name | OCTINOXATE; ZINC OXIDE |
| Strength Number | .8; .48 |
| Strength Unit | g/14g; g/14g |
| Pharmaceutical Classes |