ARTISTRY Time Defiance UV Defense SPF 50 Ultra Facial Sunscreen (Amway Corp)
Welcome to the PulseAid listing for the ARTISTRY Time Defiance UV Defense SPF 50 Ultra Facial Sunscreen drug offered from Amway Corp. This pharmaceutical is classified as a HUMAN OTC DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN OTC DRUG drug type category.
| LABELER NAME / MANUFACTURER: | Amway Corp |
| NON-PROPRIETARY NAME: | OCTINOXATE, ZINC OXIDE, OCTISALATE,TITANIUM DIOXIDE |
| SUBSTANCE NAME: | OCTINOXATE; ZINC OXIDE; OCTISALATE; TITANIUM DIOXIDE |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | TOPICAL |
| DOSAGE FORM: | CREAM |
| MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
| START MARKETING DATE: | 2012-05-10 |
| END MARKETING DATE: | 0000-00-00 |
ARTISTRY Time Defiance UV Defense SPF 50 Ultra Facial Sunscreen HUMAN OTC DRUG Details:
| Item Description | ARTISTRY Time Defiance UV Defense SPF 50 Ultra Facial Sunscreen from Amway Corp |
| LABELER NAME: | Amway Corp |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 7.5; 6.528; 5; 2.49(mL/100mL; mL/100mL; mL/100mL; mL/100mL) |
| START MARKETING DATE: | 2012-05-10 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 50390-110_eee8d16c-45bd-40a1-b3ec-f3a5dc3e2131 |
| PRODUCT NDC: | 50390-110 |
| APPLICATION NUMBER: | part352 |
Other OCTINOXATE; ZINC OXIDE; OCTISALATE; TITANIUM DIOXIDE Pharmaceutical Manufacturers / Labelers:
