An Evaluation of PDI-192 0.1% in Comparison to PDI-192 0.15% in the Treatment of Mild to Moderate Atopic Dermatitis

Inclusion Criteria:

- Subject presents with a clinical diagnosis of stable mild to moderate atopic
dermatitis.

- Subject has used the same type of soap, moisturizers, lotions, creams, ointments,
sunscreens or other skin products, and hair products (shampoo, etc.) for at least two
weeks prior to study start and agrees to continue usage with the same products and
with similar frequency for the entire study.

Exclusion Criteria:

- Subject is pregnant, lactating or is planning to become pregnant during the study.

- Subject requires any topical or systemic medications or is using topical inflammatory
dermatoses therapies that could affect the course of their atopic dermatitis during
the study period.

- Subject has used systemic corticosteroids, immunomodulators including leukotriene
inhibitors, or antimetabolites within 30 days prior to study start.

- Subject has used Ultraviolet Light Therapy (PUVA, UVB, etc.) within 30 days prior to
study start.

- Subject has used topical therapies for the treatment of (or may affect) their atopic
dermatitis including but not limited to corticosteroids, immunomodulators
(tacrolimus, pimecrolimus, etc.), tar, calcipotriene or other vitamin D preparations,
retinoids, antihistamines (doxepin, diphenhydramine, etc.), antibiotics, among
others, within 14 days prior to study start.

- Subject desires excessive or prolonged exposure to ultraviolet light (e.g., sunlight,
tanning beds) during the study.

- Subject has used systemic (oral, IV, etc.) antibiotic therapy within seven days
prior to study start.

- Subject is currently enrolled in an investigational drug or device study.

- Subject has used an investigational drug or investigational device treatment within
30 days prior to study start.