| Product NDC: | 67938-0990 |
| Proprietary Name: | Prevage Anti Agining Triple Defense Shield Broad Spectrum Sunscreen SPF 50 |
| Non Proprietary Name: | OCTINOXATE, OXYBENZONE, OCTISALATE, OCTOCRYLENE, and AVOBENZONE |
| Active Ingredient(s): | 30; 75; 50; 40; 60 mg/50mL; mg/50mL; mg/50mL; mg/50mL; mg/50mL & nbsp; OCTINOXATE, OXYBENZONE, OCTISALATE, OCTOCRYLENE, and AVOBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 67938-0990 |
| Labeler Name: | Elizabeth Arden, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20111214 |
| Package NDC: | 67938-0990-1 |
| Package Description: | 1 TUBE in 1 BOX (67938-0990-1) > 50 mL in 1 TUBE (67938-0990-2) |
| NDC Code | 67938-0990-1 |
| Proprietary Name | Prevage Anti Agining Triple Defense Shield Broad Spectrum Sunscreen SPF 50 |
| Package Description | 1 TUBE in 1 BOX (67938-0990-1) > 50 mL in 1 TUBE (67938-0990-2) |
| Product NDC | 67938-0990 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, OXYBENZONE, OCTISALATE, OCTOCRYLENE, and AVOBENZONE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20111214 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Elizabeth Arden, Inc |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 30; 75; 50; 40; 60 |
| Strength Unit | mg/50mL; mg/50mL; mg/50mL; mg/50mL; mg/50mL |
| Pharmaceutical Classes |