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 |