Product NDC: | 57913-2857 |
Proprietary Name: | Oil-Control Day SPF 15 |
Non Proprietary Name: | Avobenzone and Octinoxate |
Active Ingredient(s): | 30; 75 mg/mL; mg/mL & nbsp; Avobenzone and Octinoxate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 57913-2857 |
Labeler Name: | Erno Laszlo, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20130410 |
Package NDC: | 57913-2857-8 |
Package Description: | 1 BOTTLE in 1 CARTON (57913-2857-8) > 90 mL in 1 BOTTLE |
NDC Code | 57913-2857-8 |
Proprietary Name | Oil-Control Day SPF 15 |
Package Description | 1 BOTTLE in 1 CARTON (57913-2857-8) > 90 mL in 1 BOTTLE |
Product NDC | 57913-2857 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Avobenzone and Octinoxate |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20130410 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Erno Laszlo, Inc. |
Substance Name | AVOBENZONE; OCTINOXATE |
Strength Number | 30; 75 |
Strength Unit | mg/mL; mg/mL |
Pharmaceutical Classes |