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: | 67692-000-51 |
Package Description: | 2 mL in 1 PACKET (67692-000-51) |
NDC Code | 67692-000-51 |
Proprietary Name | Lumene Vitamin C BB Illuminating Anti-Age BB Sunscreen Broad Spectrum SPF 20 Medium |
Package Description | 2 mL in 1 PACKET (67692-000-51) |
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 |