Timewise Day Solution sunscreen SPF 35 (Mary Kay Inc.)


Welcome to the PulseAid listing for the Timewise Day Solution sunscreen SPF 35 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: Homosalate,Octisalate,Oxybenzone,Octocrylene,Avobenzone
SUBSTANCE NAME: OXYBENZONE; AVOBENZONE; OCTISALATE; HOMOSALATE; OCTOCRYLENE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: CREAM
MARKETING CATEGORY NAME: OTC MONOGRAPH NOT FINAL
START MARKETING DATE: 2012-03-01
END MARKETING DATE: 0000-00-00


Timewise Day Solution sunscreen SPF 35 HUMAN OTC DRUG Details:

Item DescriptionTimewise Day Solution sunscreen SPF 35 from Mary Kay Inc.
LABELER NAME: Mary Kay Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 1.16; .58; 1.45; 2.9; .58(mL/29mL; mL/29mL; mL/29mL; mL/29mL; mL/29mL)
START MARKETING DATE: 2012-03-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 51531-8363_ab14546e-9ffa-415d-9899-f2d60184b7f7
PRODUCT NDC: 51531-8363
APPLICATION NUMBER: part352

Other OXYBENZONE; AVOBENZONE; OCTISALATE; HOMOSALATE; OCTOCRYLENE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Mary Kay Inc.Timewise Day Solution sunscreen SPF 35