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 |