Product NDC: | 68026-533 |
Proprietary Name: | Anti-Aging Concealer SPF 20 Face Eyes Shade 30 |
Non Proprietary Name: | OCTINOXATE, OCTISALATE, OXYBENZONE |
Active Ingredient(s): | 7.5; 5; 2 mL/100mL; mL/100mL; mL/100mL & nbsp; OCTINOXATE, OCTISALATE, OXYBENZONE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68026-533 |
Labeler Name: | La Prairie, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120914 |
Package NDC: | 68026-533-75 |
Package Description: | 7.5 mL in 1 BOTTLE (68026-533-75) |
NDC Code | 68026-533-75 |
Proprietary Name | Anti-Aging Concealer SPF 20 Face Eyes Shade 30 |
Package Description | 7.5 mL in 1 BOTTLE (68026-533-75) |
Product NDC | 68026-533 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE, OCTISALATE, OXYBENZONE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20120914 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | La Prairie, Inc. |
Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE |
Strength Number | 7.5; 5; 2 |
Strength Unit | mL/100mL; mL/100mL; mL/100mL |
Pharmaceutical Classes |