Antidandruff Lotion Mediating Microbiome Rebalance

Inclusion Criteria: 1. Healthy male or female volunteer; 2. from 18 to 60 years old; 3. Skin Phototype (Fitzpatrick): I to IV; 4. Subject with hair length \> 2 cm, and preferentially shorter than shoulder length; 5. Female of childbearing potential, who is not sexually active, or using an effective contraceptive method\* for at least one month before the beginning of the study, and throughout the study or menopausal woman (with absence of menstruations for less than one year) or post-menopausal woman (with absence of menstruations for more than one year); 6. Subject exhibiting moderate to severe dandruff status of scalp at screening, pre-inclusion and inclusion visit; 7. Subject having at inclusion visit Day 0: 1. total dandruff score (adherent + non-adherent) \> or = 4.5 (ranging from 0 to 10); 2. adherent dandruff score \> or = 2.5 (ranging from 0 to 5); 3. no limit for non-adherent dandruff score (ranging from 0 to 5); 8. Subject usually using a shampoo 3 times/week and willing to have two to three times/week shampoos during the course of the study; 9. Subject agreeing to use only the supplied products during all the study; 10. Subjects agreeing to have 1 zone of less than 2x2cm2 on the scalp for non-invasive sample taking (swabs); 11. Subject agreeing to have hair shaved on 1 identified zone (1x0.5cm shaved on the high corner of each zone sampling); 12. Subject who demonstrate understanding of the study and willingness to participate as evidenced by voluntary written informed consent and have received a signed and dated copy of the informed consent form. 13. Subject affiliated to a social security or insurance system; 14. Subject willing to comply to the study requirements; 15. Subject who is willing not to take part in another clinical study in another investigating center; 16. Subject who agree to give accurate personal in personal information; 17. Subject who are able to attend all study visits. \* The effective contraceptive methods: sexually active female of childbearing potential should either be surgically sterile (oophorectomy, hysterectomy or tubal ligation), or should use a medically accepted contraceptive regimen: systemic contraceptive (oral, implant, injection), diaphragm or cervical cap with intravaginal spermicide, intravaginal device, intrauterine device (IUD), condom with spermicide. Exclusion Criteria: Edit Eligibility Criteria: Inclusions criterias: 1. Healthy male or female volunteer; 2. from 18 to 60 years old; 3. Skin Phototype (Fitzpatrick): I to IV; 4. Subject with hair length \> 2 cm, and preferentially shorter than shoulder length; 5. Female of childbearing potential, who is not sexually active, or using an effective contraceptive method\* for at least one month before the beginning of the study, and throughout the study or menopausal woman (with absence of menstruations for less than one year) or post-menopausal woman (with absence of menstruations for more than one year); 6. Subject exhibiting moderate to severe dandruff status of scalp at screening, pre-inclusion and inclusion visit; 7. Subject having at inclusion visit Day 0: 1. total dandruff score (adherent + non-adherent) \> or = 4.5 (ranging from 0 to 10); 2. adherent dandruff score \> or = 2.5 (ranging from 0 to 5); 3. no limit for non-adherent dandruff score (ranging from 0 to 5); 8. Subject usually using a shampoo 3 times/week and willing to have two to three times/week shampoos during the course of the study; 9. Subject agreeing to use only the supplied products during all the study; 10. Subjects agreeing to have 1 zone of less than 2x2cm2 on the scalp for non-invasive sample taking (swabs); 11. Subject agreeing to have hair shaved on 1 identified zone (1x0.5cm shaved on the high corner of each zone sampling); 12. Subject who demonstrate understanding of the study and willingness to participate as evidenced by voluntary written informed consent and have received a signed and dated copy of the informed consent form. 13. Subject affiliated to a social security or insurance system; 14. Subject willing to comply to the study requirements; 15. Subject who is willing not to take part in another clinical study in another investigating center; 16. Subject who agree to give accurate personal in personal information; 17. Subject who are able to attend all study visits. \* The effective contraceptive methods: sexually active female of childbearing potential should either be surgically sterile (oophorectomy, hysterectomy or tubal ligation), or should use a medically accepted contraceptive regimen: systemic contraceptive (oral, implant, injection), diaphragm or cervical cap with intravaginal spermicide, intravaginal device, intrauterine device (IUD), condom with spermicide. Non-inclusion criterias: 1. Subject with any systemic disorder or skin or scalp disease that would, in the investigator's judgment, significantly affect the interpretation of the study results (e.g. seborrheic dermatitis which shows the syndrome of invasion plaque and/or pityriasis amiantacea, atopic dermatitis, eczema or psoriasis); 2. Female subject who is known to be pregnant or who is intending to become pregnant over the duration of the study; 3. Female subject who is currently breast-feeding or have been breast-feeding in the 6 months prior to the start of the study; 4. Male subject with alopecia grade ≥ V according to Hamilton-Norwood patterns, female subject with alopecia grade I, II or III according to Ludwig patterns (Appendix 3); 5. Subject with frizzy hair influencing the scoring of dandruff; 6. Subject with significant white hair influencing the scoring of dandruff; 7. Subject who has skin marks on the scalp that could interfere with the assessments (e.g. pigmentation, tattoo, scarring etc.); 8. Subject who has used products for the scalp (dyeing, bleaching, permanent waving and straightening …) within the three weeks prior to the study; 9. Subject who has used anti-dandruff treatment (per os or topi