| Product NDC: | 50390-111 |
| Proprietary Name: | ARTISTRY YOUTH XTEND Lifting Smoothing Foundation Broad Spectrum SPF 20 Sunscreen |
| Non Proprietary Name: | OCTINOXATE, OXYBENZONE |
| Active Ingredient(s): | 75; 10 mg/mL; mg/mL & nbsp; OCTINOXATE, OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 50390-111 |
| Labeler Name: | Amway Corp |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130506 |
| Package NDC: | 50390-111-00 |
| Package Description: | 30 mL in 1 BOTTLE (50390-111-00) |
| NDC Code | 50390-111-00 |
| Proprietary Name | ARTISTRY YOUTH XTEND Lifting Smoothing Foundation Broad Spectrum SPF 20 Sunscreen |
| Package Description | 30 mL in 1 BOTTLE (50390-111-00) |
| Product NDC | 50390-111 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, OXYBENZONE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20130506 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Amway Corp |
| Substance Name | OCTINOXATE; OXYBENZONE |
| Strength Number | 75; 10 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |