| Product NDC: | 67938-1126 |
| Proprietary Name: | Prevage Anti Aging Eye Sunscreen SPF 15 |
| Non Proprietary Name: | OCTINOXATE and OXYBENZONE |
| Active Ingredient(s): | .613; .21 g/15g; g/15g & nbsp; OCTINOXATE and OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 67938-1126 |
| Labeler Name: | Elizabeth Arden, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110314 |
| Package NDC: | 67938-1126-1 |
| Package Description: | 1 JAR in 1 BOX (67938-1126-1) > 15 g in 1 JAR (67938-1126-2) |
| NDC Code | 67938-1126-1 |
| Proprietary Name | Prevage Anti Aging Eye Sunscreen SPF 15 |
| Package Description | 1 JAR in 1 BOX (67938-1126-1) > 15 g in 1 JAR (67938-1126-2) |
| Product NDC | 67938-1126 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE and OXYBENZONE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110314 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Elizabeth Arden, Inc |
| Substance Name | OCTINOXATE; OXYBENZONE |
| Strength Number | .613; .21 |
| Strength Unit | g/15g; g/15g |
| Pharmaceutical Classes |