| Eligibility |
Inclusion Criteria
- Participant must read and execute an informed consent document (that includes a HIPAA
statement) indicating that the participant has been informed of all pertinent aspects
of the trial before any assessment is performed;
- Participant must complete a Medical History Form (MHF) prior to their trial
initiation;
- Participant must be willing and able to comply with scheduled visits, treatment plan,
laboratory tests, and other trial procedures;
- Participant must agree not to expose their back to additional sunlight or tanning
beds, as either can alter the test results;
- Participant must agree not to apply any topical skin-care product to the test sites
during this trial;
- Male or female participants of childbearing potential must agree to use a highly
effective method of contraception throughout the trial and for 14 days after the last
application of assigned treatment. A participant is of childbearing potential if, in
the opinion of the investigator, he/she is biologically capable of having children and
is sexually active;
- Female participants of childbearing potential must be willing to comply with urine
pregnancy testing requirements prior to initiation of trial testing procedures and as
may be required for the duration of the trial;
- Participant must be considered dependable and capable of understanding and following
directions;
- Participant must have self-perceived Fitzpatrick skin phototype I, II, or III:
Skin Phototype Sunburn and Tanning History I Always burn easily; never tans II Always burns
easily; tans minimally III Burns moderately; tans gradually; and
- Participant must have an Individual Typology Angle value >28 degrees, determined by
the Testing Facility by colorimetric methods, within 1 week of trial participation.
Exclusion Criteria
- Participant is in ill health as determined by the Principal Investigator;
- Participant is an employee of the Clinical Division of the investigational site or a
member of their immediate family;
- Participant is a GSK CH employee directly involved in the conduct of the trial or a
member of their immediate family;
- Female participant is pregnant or intending to become pregnant over the duration of
the trial or any female participant of childbearing potential who fails to produce a
negative urine pregnancy test;
- Female participant who is lactating (self-reported);
- Participant using medication with photo-sensitizing potential;
- Participant has a history of adverse reactions or hypersensitivity to azo dyes,
cosmetics, OTC drugs, or other topical personal care products;
- Participant taking medications other than birth control that could influence the
purpose, integrity or outcome of the trial;
- Participant has used topical or systemic steroids, antihistamines, or antibiotics
within 7 days of trial initiation or during the trial;
- Participant has used anti-inflammatory medications within 7 days of trial initiation
or during the trial, that in the opinion of the PI, could interfere with the trial;
- Participant has used medication suspected of causing photobiological reactions (e.g.,
tetracyclines, thiazides, etc.), that has not been taken by the participant through a
summer season;
- Participant has a dermatological condition;
- Participant has a history of abnormal response to the sun, or a condition such as
lupus erythematosus or skin cancer;
- Participant uses tanning beds frequently;
- Participant whose test site was exposed to sunlight within the previous 4 weeks;
- Participant has a sunburn, suntan, uneven skin color, visible skin disease, scarring,
or tattoo that would interfere with evaluation of test results; Note: The presence of
non-dysplastic nevi, blemishes, or moles will be acceptable if, in the PI's judgment,
they will neither compromise the clinical trial, nor jeopardize a participant's
safety. A participant with dysplastic nevi should be disqualified.
- Participant has existing sun damage in the test site;
- Participant has excessive hair in the test area and are unwilling to have it clipped;
or
- Participant whose test sites have been used for clinical testing in which they were
exposed to ultraviolet radiation within the past 2 months.
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