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 |