Product NDC: | 67938-0904 |
Proprietary Name: | Prevage Anti Aging Moisture Broad Spectrum Sunscreen SPF 30 |
Non Proprietary Name: | OCTINOXATE, OCTISALATE, OXYBENZONE, OCTOCRYLENE, and AVOBENZONE |
Active Ingredient(s): | 10; 35; 25; 11; 25 mg/50mL; mg/50mL; mg/50mL; mg/50mL; mg/50mL & nbsp; OCTINOXATE, OCTISALATE, OXYBENZONE, OCTOCRYLENE, and AVOBENZONE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 67938-0904 |
Labeler Name: | Elizabeth Arden, Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20090604 |
Package NDC: | 67938-0904-1 |
Package Description: | 1 BOTTLE, PUMP in 1 BOX (67938-0904-1) > 50 mL in 1 BOTTLE, PUMP (67938-0904-2) |
NDC Code | 67938-0904-1 |
Proprietary Name | Prevage Anti Aging Moisture Broad Spectrum Sunscreen SPF 30 |
Package Description | 1 BOTTLE, PUMP in 1 BOX (67938-0904-1) > 50 mL in 1 BOTTLE, PUMP (67938-0904-2) |
Product NDC | 67938-0904 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE, OCTISALATE, OXYBENZONE, OCTOCRYLENE, and AVOBENZONE |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20090604 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Elizabeth Arden, Inc |
Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
Strength Number | 10; 35; 25; 11; 25 |
Strength Unit | mg/50mL; mg/50mL; mg/50mL; mg/50mL; mg/50mL |
Pharmaceutical Classes |