Age

50–75

Sex

ALL

Healthy volunteers

Accepted

1. 50-75 years
2. Willing to allow collection of 3 blood samples (Baseline, Week 12 and Week 20)
3. Willing to log daily compliance with FPP intake during the study period (12 weeks)
4. Absence of active systemic disease per investigator judgement.
5. No current use of immunosuppressant or immunomodulatory medications.
6. No active dermatological conditions at measurement sites that could impair measure, per investigator judgement.
7. Investigator determination of general good health.

1. Co-morbidity or concurrent medication that the Investigator deems impactful to patient safety or ability to adhere to FPP dosage.
2. Co-morbidity or concurrent medication that the Investigator deems confounding to outcome measure (i.e., topical or systemic steroid).
3. Current or history of allergy to FPP ingredients: Dextrose, Carica papaya, or Food yeast.
4. Concurrent participation in another interventional trial that may impact measures, per investigator judgement.
5. Uncontrolled diabetes (A1c \>7%).
6. Open wounds or actively receiving Wound Care services.
7. Pregnant or breastfeeding women.
8. Current use of warfarin.

Effect of FPP on Cutaneous Barrier Integrity