| Product NDC: | 58232-0045 |
| Proprietary Name: | Korres Quercetin 7 Oak Hydrating Antiageing and Antiwrinkle |
| Non Proprietary Name: | Octinoxate and Octocrylene |
| Active Ingredient(s): | 50; 40 mg/mL; mg/mL & nbsp; Octinoxate and Octocrylene |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 58232-0045 |
| 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: | 58232-0045-2 |
| Package Description: | 1 TUBE in 1 CARTON (58232-0045-2) > 50 mL in 1 TUBE |
| NDC Code | 58232-0045-2 |
| Proprietary Name | Korres Quercetin 7 Oak Hydrating Antiageing and Antiwrinkle |
| Package Description | 1 TUBE in 1 CARTON (58232-0045-2) > 50 mL in 1 TUBE |
| Product NDC | 58232-0045 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate and Octocrylene |
| Dosage Form Name | LOTION |
| 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 | OCTINOXATE; OCTOCRYLENE |
| Strength Number | 50; 40 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |