Product NDC: | 49967-505 |
Proprietary Name: | Yves Saint Laurent |
Non Proprietary Name: | Octinoxate |
Active Ingredient(s): | .076 g/3.8g & nbsp; Octinoxate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIPSTICK |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49967-505 |
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: | 20110801 |
Package NDC: | 49967-505-01 |
Package Description: | 1 TUBE in 1 CARTON (49967-505-01) > 3.8 g in 1 TUBE |
NDC Code | 49967-505-01 |
Proprietary Name | Yves Saint Laurent |
Package Description | 1 TUBE in 1 CARTON (49967-505-01) > 3.8 g in 1 TUBE |
Product NDC | 49967-505 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Octinoxate |
Dosage Form Name | LIPSTICK |
Route Name | TOPICAL |
Start Marketing Date | 20110801 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | L'Oreal USA Products Inc |
Substance Name | OCTINOXATE |
Strength Number | .076 |
Strength Unit | g/3.8g |
Pharmaceutical Classes |