Sun Pyrite 8X

FDA Drug Profile — Sun Pyrite 8X

Sun Pyrite 8X is listed in the FDA National Drug Code directory with 1 NDC code, marketed under brand name including Sun Pyrite 8X. Available dosage form: powder.

Drug Details

Generic Name
Sun Pyrite 8X
Brand Names
Sun Pyrite 8X
Application Number
Sponsor
Uriel Pharmacy, Inc
NDC Codes
1
Dosage Forms
POWDER
Routes
ORAL
Active Ingredients
FERROUS DISULFIDE

Indications and Usage

Directions: FOR ORAL USE ONLY.

Warnings

Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Contains lactose. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seal is broken or missing.