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 |