Ferrum Quartz

Manufacturer: Uriel Pharmacy, Inc.
Effective date: 2025-08-01
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: full-release
Hydrated at: 2026-06-01 02:34:35

Label at a glance#

ProductFerrum Quartz

Active ingredientFERROUS SULFATE, SULFUR

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 3-4 times daily with water. Ages 12 and older: 1-2 tablets. Ages 2-11: 1 tablet. Under age 2: Consult a doctor.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Each 200mg tablet contains: 40mg Ferrum sulf. (Iron sulfate) 1X, 16mg Quartz (Rock crystal) 1X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Microcrystalline cellulose, Honey, Sucrose, Magnesium stearate, Lactose

Prepared using rhythmical processes.

OTC - PURPOSE SECTION

Use: 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
Made by Uriel, East Troy, WI 53120
shopuriel.com Lot:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Ferrum Quartz Tablets

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-4197-4	Ferrum Quartz	250 in 1 BOTTLE, GLASS	TABLET	250		4

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

Ferrum Quartz
MICROCRYSTALLINE CELLULOSE
FERROUS SULFATE
FERROUS CATION
MAGNESIUM STEARATE
SULFUR
SUCROSE
LACTOSE, UNSPECIFIED FORM
HONEY

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
48951-4197	48951-4197-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
MICROCRYSTALLINE CELLULOSE	OP1R32D61U	IACT
FERROUS SULFATE	39R4TAN1VT	ACTIM
MAGNESIUM STEARATE	70097M6I30	IACT
SULFUR	70FD1KFU70	ACTIB
SUCROSE	C151H8M554	IACT
LACTOSE, UNSPECIFIED FORM	J2B2A4N98G	IACT
HONEY	Y9H1V576FH	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
Ferrum Quartz	FERRUM QUARTZ	Uriel Pharmacy, Inc.	052f687f-2263-9476-e063-6394a90a6ee9	2025-08-01	Warnings	Exact identifier ndc (package): 48951-4197-4 ndc (product): 48951-4197 ndc11 (package): 48951419704 spl id: 3b5350ed-8f2f-6acb-e063-6394a90a52ab spl set id: 052f687f-2263-9476-e063-6394a90a6ee9

Reported adverse events (FAERS/openFDA)#

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