Mary Kay Tinted Moisturizer Sunscreen SPF 20 Beige 1 (Mary Kay Inc.)
Welcome to the PulseAid listing for the Mary Kay Tinted Moisturizer Sunscreen SPF 20 Beige 1 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: | CREAM |
| MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
| START MARKETING DATE: | 2006-08-16 |
| END MARKETING DATE: | 0000-00-00 |
Mary Kay Tinted Moisturizer Sunscreen SPF 20 Beige 1 HUMAN OTC DRUG Details:
| Item Description | Mary Kay Tinted Moisturizer Sunscreen SPF 20 Beige 1 from Mary Kay Inc. |
| LABELER NAME: | Mary Kay Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 7.5; 5; 2.4; 1.75(g/100mL; g/100mL; g/100mL; g/100mL) |
| START MARKETING DATE: | 2006-08-16 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 51531-7487_6def08dd-a088-4f17-9322-72c17c35f9f0 |
| PRODUCT NDC: | 51531-7487 |
| APPLICATION NUMBER: | part352 |
Other OCTINOXATE; OCTISALATE; ZINC OXIDE; OXYBENZONE Pharmaceutical Manufacturers / Labelers:
