| Product NDC: | 49967-593 |
| Proprietary Name: | Yves Saint Laurent |
| Non Proprietary Name: | Ensulizole Octinoxate |
| Active Ingredient(s): | 1; 3.745 mL/50mL; mL/50mL & nbsp; Ensulizole Octinoxate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 49967-593 |
| Labeler Name: | L'Oreal USA Products Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120201 |
| Package NDC: | 49967-593-01 |
| Package Description: | 1 BOTTLE, PUMP in 1 CARTON (49967-593-01) > 50 mL in 1 BOTTLE, PUMP |
| NDC Code | 49967-593-01 |
| Proprietary Name | Yves Saint Laurent |
| Package Description | 1 BOTTLE, PUMP in 1 CARTON (49967-593-01) > 50 mL in 1 BOTTLE, PUMP |
| Product NDC | 49967-593 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ensulizole Octinoxate |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20120201 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | L'Oreal USA Products Inc |
| Substance Name | ENSULIZOLE; OCTINOXATE |
| Strength Number | 1; 3.745 |
| Strength Unit | mL/50mL; mL/50mL |
| Pharmaceutical Classes |