| Product NDC: | 67938-1094 |
| Proprietary Name: | Eight Hour Cream Sun Defense for Face SPF 50 Sunscreen |
| Non Proprietary Name: | Zinc Oxide |
| Active Ingredient(s): | 3.922; 2.65; 6.159 g/53g; g/53g; g/53g & nbsp; Zinc Oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 67938-1094 |
| Labeler Name: | Elizabeth Arden, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20101214 |
| Package NDC: | 67938-1094-1 |
| Package Description: | 1 TUBE in 1 BOX (67938-1094-1) > 53 g in 1 TUBE (67938-1094-2) |
| NDC Code | 67938-1094-1 |
| Proprietary Name | Eight Hour Cream Sun Defense for Face SPF 50 Sunscreen |
| Package Description | 1 TUBE in 1 BOX (67938-1094-1) > 53 g in 1 TUBE (67938-1094-2) |
| Product NDC | 67938-1094 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Zinc Oxide |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20101214 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Elizabeth Arden, Inc |
| Substance Name | OCTINOXATE; OCTISALATE; ZINC OXIDE |
| Strength Number | 3.922; 2.65; 6.159 |
| Strength Unit | g/53g; g/53g; g/53g |
| Pharmaceutical Classes |