Label: SUN PYRITE 17X liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved homeopathic

DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

Drug Label Information

Updated March 25, 2025

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  • INDICATIONS & USAGE
    Directions: FOR ORAL USE ONLY.
  • DOSAGE & ADMINISTRATION
    Take 3-4 times daily. Ages 12 and older: 10 drops. Ages 2-11: 5 drops. Under age 2: Consult a doctor.
  • ACTIVE INGREDIENT
    Active Ingredient: Sun Pyrite (Naturaliron sulfide) 17X
  • INACTIVE INGREDIENT
    Inactive Ingredients: Distilled water, 20% Organic cane alcohol, Lactose - Prepared using rhythmical processes.
  • PURPOSE
    Use: Temporary relief of headaches.
  • KEEP OUT OF REACH OF CHILDREN
    KEEP OUT OF REACH OF CHILDREN.
  • WARNINGS
    Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Contains traces of lactose. Consult a doctor ...
  • QUESTIONS
    Questions? Call 866.642.2858 - Made with care by Uriel, East Troy, WI 53120 - shopuriel.com Lot:
  • PRINCIPAL DISPLAY PANEL
    Sun Pyrite 17X Liquid
  • INGREDIENTS AND APPEARANCE
    Product Information
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