| Product NDC: | 49967-105 |
| Proprietary Name: | Dermablend Professional SkinPerfector Redness Reducing Primer Sunscreen |
| Non Proprietary Name: | Avobenzone, Octisalate and Octocrylene |
| Active Ingredient(s): | 20; 33; 46 mg/mL; mg/mL; mg/mL & nbsp; Avobenzone, Octisalate and Octocrylene |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 49967-105 |
| 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: | 20130301 |
| Package NDC: | 49967-105-01 |
| Package Description: | 1 TUBE in 1 CARTON (49967-105-01) > 30 mL in 1 TUBE |
| NDC Code | 49967-105-01 |
| Proprietary Name | Dermablend Professional SkinPerfector Redness Reducing Primer Sunscreen |
| Package Description | 1 TUBE in 1 CARTON (49967-105-01) > 30 mL in 1 TUBE |
| Product NDC | 49967-105 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Octisalate and Octocrylene |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20130301 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | L'Oreal USA Products Inc |
| Substance Name | AVOBENZONE; OCTISALATE; OCTOCRYLENE |
| Strength Number | 20; 33; 46 |
| Strength Unit | mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |