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 DescriptionMary Kay Tinted Moisturizer Sunscreen SPF 20 Bronze 2 (Drug Facts) from Mary Kay Inc.
LABELER NAME: Mary Kay Inc.
DEA SCHEDULE:
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:

Manufacturer / LabelerProprietary Name
Mary Kay Inc.Mary Kay TimeWise Day Solution Sunscreen SPF 25