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 |