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FDA Disclaimer

Important regulatory disclosures about VisioCore as a dietary supplement.

Last updated: January 1, 2026

Dietary Supplement Statement

VisioCore is a dietary supplement. The statements made about VisioCore on this website, in marketing materials, and on the product label have not been evaluated by the United States Food and Drug Administration (FDA). VisioCore is not intended to diagnose, treat, cure, or prevent any disease.

Not a Substitute for Medical Care

The information on this Site is provided for general educational and informational purposes only. It is not a substitute for advice from a qualified healthcare provider. Always consult your physician or other licensed medical professional:

Individual Results Vary

Testimonials, case studies, and personal experiences shared on this Site reflect the experiences of the individuals quoted. Results vary from person to person. No outcome is guaranteed, implied, or promised. The publication of a testimonial is not an endorsement of any specific result.

Conditions Requiring Medical Care

VisioCore is a nutritional product and is not appropriate as the sole approach to managing any diagnosed eye condition. If you have been diagnosed with macular degeneration, glaucoma, cataracts, diabetic retinopathy, or any other condition affecting your vision, please continue to follow the care plan provided by your ophthalmologist or optometrist. Do not stop or modify any prescribed treatment without medical guidance.

Pregnancy, Nursing, and Special Populations

Pregnant or nursing individuals, anyone scheduled for surgery, and anyone taking prescription medication should consult a healthcare provider before starting VisioCore. VisioCore is formulated for adults over 18 and is not intended for children.

Allergens and Sensitivities

While VisioCore is formulated to be free of major allergens, individuals with known sensitivities should review the full ingredient list before use. If you experience an unexpected reaction, stop use and contact a healthcare provider.

Manufacturing Quality

VisioCore is manufactured in the United States in a facility that is registered with the U.S. Food and Drug Administration and operated under current Good Manufacturing Practice (cGMP) standards. FDA registration of a manufacturing facility means the facility has notified the FDA of its operations; it does not constitute FDA approval or endorsement of the product itself.

Questions

If you have any questions about the safety or appropriate use of VisioCore, please contact us at support@tryvisiocore.com or (888) 996-4479. For questions about your specific health situation, always consult a licensed medical professional.