| Product NDC: | 49967-549 |
| Proprietary Name: | Lancome Paris Star Bronzer |
| Non Proprietary Name: | Octinoxate |
| Active Ingredient(s): | .975 g/13g & nbsp; Octinoxate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 49967-549 |
| 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: | 20110415 |
| Package NDC: | 49967-549-01 |
| Package Description: | 1 CONTAINER in 1 CARTON (49967-549-01) > 13 g in 1 CONTAINER |
| NDC Code | 49967-549-01 |
| Proprietary Name | Lancome Paris Star Bronzer |
| Package Description | 1 CONTAINER in 1 CARTON (49967-549-01) > 13 g in 1 CONTAINER |
| Product NDC | 49967-549 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate |
| Dosage Form Name | POWDER |
| Route Name | TOPICAL |
| Start Marketing Date | 20110415 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | L'Oreal USA Products Inc |
| Substance Name | OCTINOXATE |
| Strength Number | .975 |
| Strength Unit | g/13g |
| Pharmaceutical Classes |