A Clinical Study to Assess the Safety and Effectiveness of Test Product in Healthy Adult Human Subjects With Dry or Sensitive Skin

Inclusion Criteria

• •Age: 18 to 55 years (both inclusive) at the time of consent.
• •Sex: Healthy male and non-pregnant/non-lactating females.
• •Females of childbearing potential must have a self-reported negative pregnancy test.
• •Subject are generally in good health.
• •Subject with dry or sensitive skin at a time of screening. (Dermatological Assessment)
• •Subjects assessment site must be free of cuts, tattoos, scratches, abrasions, scars, uneven skin tone, sunburn, excessive tan, excessive hair or open wounds.
• •Subject is able to remain on stable doses of contraceptive or replacement hormonal therapy, including no therapy, 6 weeks prior to and for the duration of the study.
• •If the subject is of childbearing potential, is practicing and agrees to maintain an established method of birth control (IUD, hormonal implant device/injection, regular use of birth control pills or patch, diaphragm, condoms with spermicide or sponge with spermicidal jelly, cream or foam, partner vasectomy or abstinence). Females will be considered as non-childbearing potential if they are surgically sterile, have been post-menopausal for at least 1 year or have had a tubal ligation.
• •Subjects are willing to give written informed consent and are willing to come for regular follow up.
• •Subjects who commit not to use medicated skincare products other than the test product for the entire duration of the study.
• •Subject who have not participated in a similar investigation in the past three months.
• •Willing to use test product throughout the study period.