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 |