| Product NDC: | 68828-131 |
| Proprietary Name: | Daily Defense SPF 15 |
| Non Proprietary Name: | Octinoxate, Zinc Oxide |
| Active Ingredient(s): | 7.5; 3 g/100mL; g/100mL & nbsp; Octinoxate, Zinc Oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 68828-131 |
| Labeler Name: | Jafra Cosmetics International Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120530 |
| Package NDC: | 68828-131-02 |
| Package Description: | 1 JAR in 1 CARTON (68828-131-02) > 50 mL in 1 JAR (68828-131-01) |
| NDC Code | 68828-131-02 |
| Proprietary Name | Daily Defense SPF 15 |
| Package Description | 1 JAR in 1 CARTON (68828-131-02) > 50 mL in 1 JAR (68828-131-01) |
| Product NDC | 68828-131 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate, Zinc Oxide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120530 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Jafra Cosmetics International Inc |
| Substance Name | OCTINOXATE; ZINC OXIDE |
| Strength Number | 7.5; 3 |
| Strength Unit | g/100mL; g/100mL |
| Pharmaceutical Classes |