Expired Study
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Union, New Jersey 07083


Purpose:

To evaluate the Sun Protection Factor efficacy on human skin.


Criteria:

Inclusion Criteria: - Fitzpatrick Skin Type l, ll and/or lll for UVB testing. - Fitzpatrick Skin Type ll, lll and/or lV for UVA testing. - Male and female - Aged between 18-70 years old. - Good health as determined from the HRL SHF - Signed and dated Informed Consent Form - Signed and dated HIPAA Form - An unambiguous MED or MPPD (Minimal Persistent Pigment Darkening Dose) Exclusion Criteria: - Subjects on test at any other research laboratory or clinic. - Known allergy or sensitivity to sunscreens, cosmetics and toiletries, topical drugs and/or ultraviolet light. - Pre-existing dermatologic conditions which have been dianoses by a medical professional (e.g. psoriasis, eczema, etc.) which would interfere with this study. - Pre-existing other medical conditions (e.g. adult asthma. diabetes). - Treatment with antihistamines or corticosteroids within one week prior to initiation of the test. - Treatment with antibiotics within two weeks prior to initiation of the test. - Chronic medication which could affect the results of the study. - Known pregnant or nursing women.


NCT ID:

NCT02823509


Primary Contact:

Study Director
Bayer Study Director
Bayer


Backup Contact:

N/A


Location Contact:

Union, New Jersey 07083
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: February 04, 2019

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