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 |