| Product NDC: | 76280-197 |
| Proprietary Name: | Julep daylight defense for hands and face |
| Non Proprietary Name: | Octinoxate, Oxybenzone, Zinc Oxide, Esulizole |
| Active Ingredient(s): | 2; 7.5; 4; 3 g/100mL; g/100mL; g/100mL; g/100mL & nbsp; Octinoxate, Oxybenzone, Zinc Oxide, Esulizole |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 76280-197 |
| Labeler Name: | Julep Nail Parlor Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120601 |
| Package NDC: | 76280-197-01 |
| Package Description: | 89 mL in 1 TUBE (76280-197-01) |
| NDC Code | 76280-197-01 |
| Proprietary Name | Julep daylight defense for hands and face |
| Package Description | 89 mL in 1 TUBE (76280-197-01) |
| Product NDC | 76280-197 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate, Oxybenzone, Zinc Oxide, Esulizole |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120601 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Julep Nail Parlor Company |
| Substance Name | ENSULIZOLE; OCTINOXATE; OXYBENZONE; ZINC OXIDE |
| Strength Number | 2; 7.5; 4; 3 |
| Strength Unit | g/100mL; g/100mL; g/100mL; g/100mL |
| Pharmaceutical Classes |