| Product NDC: | 67692-811 |
| Proprietary Name: | Lumene Time Freeze Anti-Age CC Color Correcting SPF 20 Sunscreen Broad Spectrum MEDIUM |
| Non Proprietary Name: | OCTINOXATE, TITANIUM DIOXIDE |
| Active Ingredient(s): | 40; 8.3 mg/mL; mg/mL & nbsp; OCTINOXATE, TITANIUM DIOXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 67692-811 |
| Labeler Name: | LUMENE OY |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130409 |
| Package NDC: | 67692-811-00 |
| Package Description: | 1 TUBE in 1 PACKAGE (67692-811-00) > 30 mL in 1 TUBE |
| NDC Code | 67692-811-00 |
| Proprietary Name | Lumene Time Freeze Anti-Age CC Color Correcting SPF 20 Sunscreen Broad Spectrum MEDIUM |
| Package Description | 1 TUBE in 1 PACKAGE (67692-811-00) > 30 mL in 1 TUBE |
| Product NDC | 67692-811 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, TITANIUM DIOXIDE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20130409 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | LUMENE OY |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
| Strength Number | 40; 8.3 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |