Product NDC: | 49967-452 |
Proprietary Name: | Maybelline New York |
Non Proprietary Name: | Octinoxate Octisalate |
Active Ingredient(s): | .33; .132 g/4.4g; g/4.4g & nbsp; Octinoxate Octisalate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIPSTICK |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49967-452 |
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: | 49967-452-01 |
Package Description: | 1 TUBE in 1 BLISTER PACK (49967-452-01) > 4.4 g in 1 TUBE |
NDC Code | 49967-452-01 |
Proprietary Name | Maybelline New York |
Package Description | 1 TUBE in 1 BLISTER PACK (49967-452-01) > 4.4 g in 1 TUBE |
Product NDC | 49967-452 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Octinoxate Octisalate |
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; OCTISALATE |
Strength Number | .33; .132 |
Strength Unit | g/4.4g; g/4.4g |
Pharmaceutical Classes |