| Product NDC: | 67692-000 |
| Proprietary Name: | Lumene Vitamin C BB Illuminating Anti-Age BB Sunscreen Broad Spectrum SPF 20 Medium |
| Non Proprietary Name: | OCTINOXATE |
| Active Ingredient(s): | 6 mL/100mL & nbsp; OCTINOXATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 67692-000 |
| Labeler Name: | Lumene Oy |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120808 |
| Package NDC: | 67692-000-50 |
| Package Description: | 50 mL in 1 BOTTLE (67692-000-50) |
| NDC Code | 67692-000-50 |
| Proprietary Name | Lumene Vitamin C BB Illuminating Anti-Age BB Sunscreen Broad Spectrum SPF 20 Medium |
| Package Description | 50 mL in 1 BOTTLE (67692-000-50) |
| Product NDC | 67692-000 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120808 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Lumene Oy |
| Substance Name | OCTINOXATE |
| Strength Number | 6 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |