None listed
Conditions
Interventions
Intervention1: Test Product: S-5 Nutritonal Supplement: Quantity 1 Sachet in 500ml of warm water. Route of administration: oral Frequency: Once Duration:30 days
Control Intervention1: Not Applicable:
Sponsors
Silphion Research Pvt Ltd
Eligibility
Inclusion criteria
Inclusion criteria: 1) Gender: Male or Female with age 20-45 2) Subjects willing to give written informed consent 3) Women of child bearing potential must have a negative urine pregnancy test prior to study entry. 4) 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 adverse events.
Exclusion criteria
Exclusion criteria: 1. Pregnant or nursing mothers 2.Volunteers on log term medication 3.Individual taking currently any supplements 4.Individual indergoing any skin related treatments 5.Chronic illness which may influence the outcome of the study 6.Subjects on any medical treatment either systemic or topical which may interfere with the performance of the study treatment (presently or in the past 1 month) 7.Subject in an exclusion period or participating in another food, cosmetic or therapeutic trial.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Change in Melanin Index 2. Change in Lightning Index 3. Change in Hydration 4. ITA 5. CBC 6. RFT 7. LFTTimepoint: Time Points At Day 0, At Day 14, At Day 30 | — |
Secondary
| Measure | Time frame |
|---|---|
| Not ApplicableTimepoint: Not Applicable | — |
Countries
India
Contacts
Public ContactPuneet Mittal
CCFT Laboratories
Outcome results
None listed