A Randomized, Double-blind, Parallel-group, Multicenter, Placebo-controlled Phase 2 Dose-ranging Trial of the Efficacy and Safety of a New Botanical Drug Product Containing East Indian Sandalwood Oil in the Treatment of Common Warts (Verruca Vulgaris)

Inclusion Criteria:

1. Are male or female, and 18 years of age or older at enrollment;

2. Have 2 to 10 common warts (Verruca vulgaris) to be treated within a single 5 cm-by-5
cm contiguous area (the treatment area);

3. The treatment area can be located anywhere on the body except for the following
prohibited areas: the eye area (including eyelids), lips, mouth cavity, nasal cavity,
inner ear, palms of the hands, soles of the feet, or the anogenital area;

4. The total surface area of the warts to be treated is ≤600 mm2;

5. If female of childbearing potential, have a negative urine pregnancy test at
Screening and Randomization/Day 1, and are willing to use effective contraception
during the study (ie, oral, implanted, or injectable contraceptives, intrauterine
device (IUD), diaphragm, condom, tubal ligation, abstinence, or are in a monogamous
relationship with a partner who has had a vasectomy);

6. Are judged to be in good health based upon the results of a physical examination,
medical history, and safety laboratory tests;

7. Are willing and able to provide written informed consent;

8. Agree to use no wart-removing product (prescription or over-the-counter [OTC]) other
than the study product during the course of the study;

9. Are willing and able to comply with the requirements of the study;

10. Are free of any systemic or dermatologic disorder, which, in the opinion of the
investigator, will interfere with the study results or increase the risk of AEs.

11. Are willing to refrain from using cosmetics or other topical products in the
treatment area for the duration of the study.

Exclusion Criteria:

1. Have less than 2 or more than 10 common warts within the designated treatment area;

2. Have warts outside of the treatment area that would interfere with study procedures
or analyses;

3. Have participated in an investigational trial within 30 days prior to enrollment;

4. Have participated in a prior trial investigating EISO use for the treatment of common
warts;

5. Have used salicylic acid or any over-the-counter wart-removing product in the
treatment area within 30 days prior to enrollment;

6. Have used or will use oral zinc and/or cimetidine within 30 days prior to enrollment
or during the course of the study;

7. Have received cryotherapy in the treatment area within 60 days prior to enrollment;

8. Have required or will require systemic intake of immunosuppressive or
immunomodulatory medication (including oral or parenteral corticosteroids) within 30
days prior to enrollment or during the course of the study. Routine use of inhaled or
intranasal corticosteroids during the study is allowed;

9. Have any current and/or recurrent pathologically relevant skin infections in the
treatment area other than common warts (with the exception of Herpes simplex virus
labialis);

10. Have any current uncontrolled infection;

11. Are pregnant, plan to become pregnant, or are breastfeeding;

12. Have a known sensitivity to any of the constituents of the investigational or control
products including sandalwood oil, fragrances, or any members of the Compositae
family of vascular plants (eg, sunflowers, daisies, dahlias, etc.);

13. Have any chronic or acute medical condition that, in the opinion of the investigator,
may interfere with the study results or place the subject at undue risk (including
human immunodeficiency virus, systemic lupus erythematosis, viral hepatitis, etc.);

14. Have any active malignancy or are undergoing treatment for any malignancy other than
nonmelanoma skin cancer;

15. Have, in the opinion of the investigator, clinically significant clinical laboratory
results at the time of screening that may interfere with the study results or place
the subject at undue risk.