Product NDC: | 67692-810 |
Proprietary Name: | Lumene Time Freeze Anti-Age CC Color Correcting SPF 20 Sunscreen Broad Spectrum LIGHT |
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: | 67692-810 |
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: | 67692-810-00 |
Package Description: | 1 TUBE in 1 PACKAGE (67692-810-00) > 30 mL in 1 TUBE |
NDC Code | 67692-810-00 |
Proprietary Name | Lumene Time Freeze Anti-Age CC Color Correcting SPF 20 Sunscreen Broad Spectrum LIGHT |
Package Description | 1 TUBE in 1 PACKAGE (67692-810-00) > 30 mL in 1 TUBE |
Product NDC | 67692-810 |
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 |