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 |