A Clinical Trial to Evaluate Efficacy and Safety of a Water-soluble Head Lice Product.

The present study is set-up to compare in vivo clinical performance and safety of the test
product versus an in the US commercially available, pyrethrum-based product (RID® shampoo).
The study will be performed in subjects ≥2 year of both genders with confirmed diagnosis of
head lice infestation. To support safety, local and global tolerability, skin and ocular
irritation will be assessed and adverse events (AEs) will be registered.

Inclusion Criteria:

1. Gender: male / female.

2. Women of childbearing potential is a premenopausal female that is anatomically and
physiologically capable of becoming pregnant following menarche.

Female subjects: are women of childbearing potential who test negative for pregnancy
and agree to use a reliable method of birth control or remain abstinent during the
study. Methods of contraception considered acceptable include oral contraceptives,
contraceptive patch, intrauterine device, vaginal ring, diaphragm with contraceptive
gel, or condom with contraceptive gel

- or are women of non-childbearing potential, defined as: women who have had
surgical sterilization (hysterectomy, bilateral oophorectomy, or tubal ligation),

- or women who are ≥60 years of age.

3. Age: ≥ 2 year of age at the time of enrollment.

4. Subject must have an active head lice infestation defined as at least 5 live lice
(adults and/or nymphs) and 5 apparently live nits, present on the scalp and/or hair,
as determined by a trained evaluator.

5. Subject is in good general health based on medical history.

6. The subject or his/her parent/legal guardian must give written informed consent, after
having been oral and written informed about benefits and potential risks of the trial,
as well as information regarding the insurance, taken out to cover the subjects
participating in the study. A caregiver must sign an informed consent agreement for
children not old enough to do so. Children ages 6-18 years of age will be administered
a child's assent form. Subject or his/her parent/legal guardian must be capable of
understanding and providing written informed consent.

7. Following application and rinsing of the test products, subject agrees not to shampoo,
wash, or rinse their hair or scalp until the 24-hour post treatment evaluation has
been completed.

8. The subject agrees not to cut or chemically treat their hair while participating in
the study.

9. No more than one working male per household may be excluded from evaluation if he is
assessed as being lice free by himself or caregiver.

10. Subject agrees to follow all study instructions, including attending all follow-up
appointments.

11. Agree to not use any other pediculicides or medicated hair grooming products for the
duration of the study (through Day 10 visit).

12. The parent or legal guardian of a child must be willing to have other family members
screened for head lice. If other household members are found to have head lice and are
eligible, they must be either enrolled in the study OR receive the standard of care at
the site and in the same manner as study participants.

13. Have a single place of residence.

14. The subject or his/her parent or legal guardian must give written informed consent,
after having been oral and written informed about benefits and potential risks of the
trial, as well as details of the insurance taken out to cover the subjects
participating in the study

15. Subjects must agree to not use any other ant-lice treatment for the duration of the
study

Exclusion Criteria:

1. Application of any form of head lice treatment, whether prescription or
over-the-counter (OTC), or home remedy for 30 days prior to their screening visit (Day
1).

2. Application of any topical medication of any kind on the hair for a period of 48 hours
prior to the screening visit.

3. Use of systemic or topical drugs or medications, including systemic antibiotics, which
in the opinion of the investigative personnel may interfere with the study results.

4. Known skin allergies, multiple drug allergies or multiple allergies to cosmetic
products.

5. History of allergy or hypersensitivity to ragweed, active ingredients or constituents
of the test products.

6. Subject with any visible skin/scalp condition at the treatment site which, in the
opinion of the investigative personnel, will interfere with the evaluation of the test
product.

7. Subjects with chronic scalp disorder.

8. Subject or his/her legal guardian who, in the opinion of the investigative personnel,
do not understand the subject requirements for study participations and/or may be
likely to exhibit poor compliance with the required visits.

9. Females who are pregnant or nursing.

10. Hair longer than mid-back.

11. Subject suspected or known not to follow instructions

12. Previous participation in this study or participation in any other investigational
trial within the preceding 30 days

13. The subject is directly affiliated to the investigator site personnel and/or their
immediate families. Immediate family is defined as a spouse, parent, child, or
sibling, whether biological or legally adopted

14. The subject is an Oystershell employee or is an employee of a third-party
organizations involved in the study.