Mary Kay Tinted Moisturizer Sunscreen SPF 20 Bronze 2 (Drug Facts) (Mary Kay Inc.)
Welcome to the PulseAid listing for the Mary Kay Tinted Moisturizer Sunscreen SPF 20 Bronze 2 (Drug Facts) 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 FINAL |
START MARKETING DATE: | 2012-06-12 |
END MARKETING DATE: | 0000-00-00 |
Mary Kay Tinted Moisturizer Sunscreen SPF 20 Bronze 2 (Drug Facts) HUMAN OTC DRUG Details:
Item Description | Mary Kay Tinted Moisturizer Sunscreen SPF 20 Bronze 2 (Drug Facts) from Mary Kay Inc. |
LABELER NAME: | Mary Kay Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 7.5; 5; 2.43; 1.75(g/100mL; g/100mL; g/100mL; g/100mL) |
START MARKETING DATE: | 2012-06-12 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 51531-4333_0095e08f-dc9a-48a9-bd8f-0eb63f878d8d |
PRODUCT NDC: | 51531-4333 |
APPLICATION NUMBER: | part352 |
Other OCTINOXATE; OCTISALATE; ZINC OXIDE; OXYBENZONE Pharmaceutical Manufacturers / Labelers: