Product NDC: | 67692-361 |
Proprietary Name: | LUMENE TIME FREEZE FIRMING DAY SPF 15 |
Non Proprietary Name: | AVOBENZONE, OCTINOXATE, OCTISALATE, OXYBENZONE |
Active Ingredient(s): | 30; 75; 40; 50 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; AVOBENZONE, OCTINOXATE, OCTISALATE, OXYBENZONE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 67692-361 |
Labeler Name: | LUMENE OY |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20101119 |
Package NDC: | 67692-361-01 |
Package Description: | 15 mL in 1 JAR (67692-361-01) |
NDC Code | 67692-361-01 |
Proprietary Name | LUMENE TIME FREEZE FIRMING DAY SPF 15 |
Package Description | 15 mL in 1 JAR (67692-361-01) |
Product NDC | 67692-361 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | AVOBENZONE, OCTINOXATE, OCTISALATE, OXYBENZONE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20101119 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | LUMENE OY |
Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE; OXYBENZONE |
Strength Number | 30; 75; 40; 50 |
Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
Pharmaceutical Classes |