Sun Pyrite 8X

Manufacturer: Uriel Pharmacy, Inc
Effective date: 2025-02-21
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:32:20

Label at a glance#

ProductSun Pyrite 8X

Active ingredientFERROUS DISULFIDE

Label structure9 sections

Contacts and useful links#

PhoneLabel contact866.642.2858

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR ORAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

Take in the morning. Ages 12 and older: 1/8 teaspoon. Ages 2-11: 1/16 teaspoon. Under age 2: Consult a doctor.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Sun Pyrite (Natural iron sulfide) 8x

INACTIVE INGREDIENT SECTION

Inactive Ingredient: Lactose

Prepared using rhythmical processes.

OTC - PURPOSE SECTION

Uses: Temporary relief of headache.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

WARNINGS SECTION

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.

OTC - QUESTIONS SECTION

Questions? Call 866.642.2858
Uriel, East Troy, WI 53120
shopuriel.com Lot:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Sun Pyrite 8X Powder

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-8433-4	Sun Pyrite 8X	50 g in 1 BOTTLE	POWDER	50		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-8433	SUN PYRITE 8X POWDER [URIEL PHARMACY, INC]	1	Current NDC, 1 package rows	20250309_2eae3f2d-b711-0f50-e063-6294a90a8349.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

Sun Pyrite 8X
FERROUS DISULFIDE
FERROUS CATION
LACTOSE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
48951-8433	48951-8433-4

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
FERROUS DISULFIDE	132N09W4PR	ACTIM
LACTOSE	J2B2A4N98G	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Sun Pyrite 8X	SUN PYRITE 8X	Uriel Pharmacy, Inc	2eae3f2d-b711-0f50-e063-6294a90a8349	2025-02-21	Warnings	Exact identifier ndc (package): 48951-8433-4 ndc (product): 48951-8433 ndc11 (package): 48951843304 spl id: 2eae3f2d-b712-0f50-e063-6294a90a8349 spl set id: 2eae3f2d-b711-0f50-e063-6294a90a8349

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.