Product NDC: | 76209-234 |
Proprietary Name: | De-Aging Moisturizing Day Creme With Sunscreen SPF 20 |
Non Proprietary Name: | OCTINOXATE, OCTISALATE, OXYBENZONE, TITANIUM DIOXIDE |
Active Ingredient(s): | 7.5; 3; 3; .4 mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; OCTINOXATE, OCTISALATE, OXYBENZONE, TITANIUM DIOXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 76209-234 |
Labeler Name: | Market America |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110608 |
Package NDC: | 76209-234-01 |
Package Description: | 60 mL in 1 BOTTLE (76209-234-01) |
NDC Code | 76209-234-01 |
Proprietary Name | De-Aging Moisturizing Day Creme With Sunscreen SPF 20 |
Package Description | 60 mL in 1 BOTTLE (76209-234-01) |
Product NDC | 76209-234 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE, OCTISALATE, OXYBENZONE, TITANIUM DIOXIDE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20110608 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Market America |
Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE; TITANIUM DIOXIDE |
Strength Number | 7.5; 3; 3; .4 |
Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL |
Pharmaceutical Classes |