| 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 |