Product NDC: | 49967-715 |
Proprietary Name: | Maybelline New York Fit Me |
Non Proprietary Name: | Octinoxate |
Active Ingredient(s): | 2.1 mL/30mL & nbsp; Octinoxate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49967-715 |
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: | 20101101 |
Package NDC: | 49967-715-01 |
Package Description: | 30 mL in 1 BOTTLE, GLASS (49967-715-01) |
NDC Code | 49967-715-01 |
Proprietary Name | Maybelline New York Fit Me |
Package Description | 30 mL in 1 BOTTLE, GLASS (49967-715-01) |
Product NDC | 49967-715 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Octinoxate |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20101101 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | L'Oreal USA Products Inc |
Substance Name | OCTINOXATE |
Strength Number | 2.1 |
Strength Unit | mL/30mL |
Pharmaceutical Classes |