Mary Kay TimeWise Day Solution Sunscreen SPF 25 (Mary Kay Inc.)
Welcome to the PulseAid listing for the Mary Kay TimeWise Day Solution Sunscreen SPF 25 drug offered from Mary Kay Inc.. 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: | Mary Kay Inc. |
| NON-PROPRIETARY NAME: | octinoxate, octisalate, zinc oxide, oxybenzone, |
| SUBSTANCE NAME: | OCTINOXATE; OCTISALATE; ZINC OXIDE; OXYBENZONE |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | TOPICAL |
| DOSAGE FORM: | LOTION |
| MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
| START MARKETING DATE: | 2005-12-16 |
| END MARKETING DATE: | 0000-00-00 |
Mary Kay TimeWise Day Solution Sunscreen SPF 25 HUMAN OTC DRUG Details:
| Item Description | Mary Kay TimeWise Day Solution Sunscreen SPF 25 from Mary Kay Inc. |
| LABELER NAME: | Mary Kay Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 7.5; 5; 3.88; 3(g/100mL; g/100mL; g/100mL; g/100mL) |
| START MARKETING DATE: | 2005-12-16 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 51531-2326_3abec8b9-b0ed-4e97-904c-4853004f73ec |
| PRODUCT NDC: | 51531-2326 |
| APPLICATION NUMBER: | part352 |
Other OCTINOXATE; OCTISALATE; ZINC OXIDE; OXYBENZONE Pharmaceutical Manufacturers / Labelers:
