| Product NDC: | 58232-0041 |
| Proprietary Name: | Korres Wild Rose Mineral Foundation |
| Non Proprietary Name: | Titanium Dioxide and Zinc Oxide |
| Active Ingredient(s): | 16; 15 mg/g; mg/g & nbsp; Titanium Dioxide and Zinc Oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 58232-0041 |
| Labeler Name: | Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110501 |
| Package NDC: | 58232-0041-1 |
| Package Description: | 7.5 g in 1 JAR (58232-0041-1) |
| NDC Code | 58232-0041-1 |
| Proprietary Name | Korres Wild Rose Mineral Foundation |
| Package Description | 7.5 g in 1 JAR (58232-0041-1) |
| Product NDC | 58232-0041 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Titanium Dioxide and Zinc Oxide |
| Dosage Form Name | POWDER |
| Route Name | TOPICAL |
| Start Marketing Date | 20110501 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. |
| Substance Name | TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 16; 15 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes |