| Product NDC: | 67692-072 |
| Proprietary Name: | Lumene Excellent Future Age-Defying and Repairing Day SPF 15 Sunscreen |
| Non Proprietary Name: | AVOBENZONE, OCTINOXATE, OCTISALATE, OCTOCRYLENE |
| Active Ingredient(s): | 3; 6; 2; 2.7 mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; AVOBENZONE, OCTINOXATE, OCTISALATE, OCTOCRYLENE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 67692-072 |
| Labeler Name: | LUMENE OY |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120912 |
| Package NDC: | 67692-072-00 |
| Package Description: | 1 BOTTLE in 1 CARTON (67692-072-00) > 50 mL in 1 BOTTLE |
| NDC Code | 67692-072-00 |
| Proprietary Name | Lumene Excellent Future Age-Defying and Repairing Day SPF 15 Sunscreen |
| Package Description | 1 BOTTLE in 1 CARTON (67692-072-00) > 50 mL in 1 BOTTLE |
| Product NDC | 67692-072 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | AVOBENZONE, OCTINOXATE, OCTISALATE, OCTOCRYLENE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120912 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | LUMENE OY |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE; OCTOCRYLENE |
| Strength Number | 3; 6; 2; 2.7 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |