| Product NDC: | 66171-123 |
| Proprietary Name: | Dr.Denese SPF 30 Defense Day |
| Non Proprietary Name: | ZINC OXIDE, OCTINOXATE |
| Active Ingredient(s): | 7.5; 7.5 g/100g; g/100g & nbsp; ZINC OXIDE, OCTINOXATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 66171-123 |
| Labeler Name: | SkinScience Labs, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110521 |
| Package NDC: | 66171-123-02 |
| Package Description: | 45 g in 1 TUBE (66171-123-02) |
| NDC Code | 66171-123-02 |
| Proprietary Name | Dr.Denese SPF 30 Defense Day |
| Package Description | 45 g in 1 TUBE (66171-123-02) |
| Product NDC | 66171-123 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ZINC OXIDE, OCTINOXATE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110521 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | SkinScience Labs, Inc |
| Substance Name | OCTINOXATE; ZINC OXIDE |
| Strength Number | 7.5; 7.5 |
| Strength Unit | g/100g; g/100g |
| Pharmaceutical Classes |