A Study to Evaluate the Therapeutic Equivalence of Generic Permethrin Cream 5% to Elimite® in the Treatment of Scabies

1. Signed Informed Consent that meets all criteria of current FDA regulations.
2. Male or non-pregnant, non-lactating female at least 2 years of age or older.
3. Diagnosis of active scabies by presence of a burrow and/or typical scabietic lesions at the classic sites of infestation.
4. Parasitological confirmation of clinical diagnosis with demonstration under light microscope of mites and/or their products (larvae, eggs or fecal material).
5. Symptom score of 2 or 3 on a 4-point rating scale of 0-3 for nocturnal itching.

6. Women must be either 1 year post-menopausal (no menstrual periods for at least 12 months), surgically sterile, or if they are of child-bearing potential, they must:

   • Have been using systemic birth control, intrauterine device, or used barrier methods such as diaphragm plus spermicide or condom plus spermicide consistently, at least 14 days before study cream administration.
   • Had a normal menstrual cycle for the month before start of treatment.
   • Have a negative urine pregnancy test result upon entry into the study.
   • Agree to use a medically accepted form of birth control (oral, implant, injectable or transdermal contraceptives, intrauterine device, condom plus spermicide, diaphragm plus spermicide) or practice abstinence throughout the study period.
7. Free from any systemic or dermatologic disorder that, in the opinion of the Investigator, will interfere with the study results or increase the risk of adverse events.
8. Ability to apply study product to self or to other person if a child. If patient is a child, then parent/guardian will apply study product to him/her.

Exclusion Criteria:

1. Known hypersensitivity to permethrin cream or any of its components, ragweed or chrysanthemums, synthetic pyrethroids or pyrethrin.
2. Use of any systemic or topical acaricide 1 month before enrollment.
3. Patients with crusted/Norwegian scabies.
4. Patients with an underlying immunodeficient state (including prolonged treatment with corticosteroids), immunosuppressive disorders requiring therapy, severe systemic disease and history of HIV infection.
5. Any condition, medical, psychological, or social, that, in the Investigator's opinion, would interfere with participation in the study.
6. Women who are pregnant, planning pregnancy or lactating.
7. Family members of employees of the clinic or Investigator.
8. Patients who, in the opinion of the Investigator, would be non-compliant with the requirements of the study protocol.
9. Patients whose close personal contacts will not or are not willing to comply with standard of care for Scabies management.
10. Patients less than 2 years of age.
11. Patients or guardians of patients, who are unable or unwilling to give informed consent or assent respectively.
12. Receipt of any drug as part of a research study within 30 days before screening.
13. History of seizures.
14. Severe cutaneous bacterial or fungal infections requiring therapy (including systemic and topical antibiotics) or coexisting dermatological disorder that could interfere with the diagnosis and subsequent monitoring of scabies.
15. Treatment with systemic or topical corticosteroids less than 2 weeks and less than 1 week from enrollment, respectively.