A Twelve Week Clinical Study to Evaluate the Efficacy and Tolerability of a Sunscreen Moisturizer SPF 50+

Inclusion Criteria: * Women between the ages of 35 and 60 years * Women with Fitzpatrick skin type I-VI * Subjects must have moderate to severe overall facial photodamage * Subjects must have no known medical conditions that, in the investigator's opinion, may interfere with study participation. * Subjects must be willing to provide verbal understanding and written informed consent. Exclusion Criteria: * Subjects who have demonstrated a previous hypersensitivity reaction to any of the ingredients in the study product(s). * Subjects who are currently under a physician's care for a medical problem that, in the opinion of the Investigator or his designee, could affect the subject's treatment response. * Subjects who are nursing, pregnant, or planning a pregnancy during this study * Subjects who have a health condition and/or pre-existing or dormant dermatologic disease on the face * Subjects who are not willing to avoid daily sun exposure on their face and the use of tanning beds or sunless tanning products during the duration of the study. * Is currently taking or have taken within the listed time frame prior to the start of the study: Oral isotretinoin (Accutane®) within the last 6 months; Avita®, Differin®, Renova®, Retin-A®, Retin-A Micro®, Soriatane®, or Tazorac® within 3 months; Prescription-strength skin-lightening products within 4 months; Any anti-wrinkle, skin-lightening, or other product or topical or systemic medication known to affect skin aging or dyschromia wit…