| 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 |