Product NDC: | 51531-4189 |
Proprietary Name: | Foundation Primer SPF 15 |
Non Proprietary Name: | Titanium Dioxide , Zinc Oxide , Octinoxate |
Active Ingredient(s): | .7; .222; 2.73 g/14g; g/14g; g/14g & nbsp; Titanium Dioxide , Zinc Oxide , Octinoxate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51531-4189 |
Labeler Name: | Mary Kay Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20091111 |
Package NDC: | 51531-4189-0 |
Package Description: | 14 g in 1 CONTAINER (51531-4189-0) |
NDC Code | 51531-4189-0 |
Proprietary Name | Foundation Primer SPF 15 |
Package Description | 14 g in 1 CONTAINER (51531-4189-0) |
Product NDC | 51531-4189 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Titanium Dioxide , Zinc Oxide , Octinoxate |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20091111 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Mary Kay Inc. |
Substance Name | OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE |
Strength Number | .7; .222; 2.73 |
Strength Unit | g/14g; g/14g; g/14g |
Pharmaceutical Classes |