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 |