Scorodite 6X Special Order

Manufacturer: Uriel Pharmacy Inc.
Effective date: 2019-12-09
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:11:37

Label at a glance#

ProductScorodite 6X Special Order

Active ingredientFERROUS ARSENATE

Label structure9 sections

Contacts and useful links#

PhoneLabel contact866.642.2858

Websitewww.urielpharmacy.com

www.urielpharmacy.com

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR ORAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

Take 3-4 times daily. 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: Ferrum arsenicosum (Iron arsenite solution) 6X

INACTIVE INGREDIENT SECTION

Inactive Ingredient: Lactose

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
Uriel, East Troy, WI 53120
www.urielpharmacy.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Scorodite 6X special Order Powder

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
48951-8363-4	2025-01-30	C162847	48780-1	2cef2736-b027-d83d-e063-dadaa90ab31f	Scorodite 6X Special Order

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-8363-4	Scorodite 6X Special Order	50 g in 1 BOTTLE, GLASS	POWDER	50		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-8363	SCORODITE 6X SPECIAL ORDER POWDER [URIEL PHARMACY INC.]	1	Legacy NDC, 1 package rows	20191210_994b65d2-4392-6d87-e053-2a95a90a1fc3.zip

Products#

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

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

Scorodite 6X Special Order
LACTOSE, UNSPECIFIED FORM
ANHYDROUS LACTOSE
FERROUS ARSENATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
48951-8363	48951-8363-4

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
LACTOSE, UNSPECIFIED FORM	J2B2A4N98G	IACT
FERROUS ARSENATE	129CO35H12	ACTIB

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
994b65d2-4393-6d87-e053-2a95a90a1fc3			994b65d2-4392-6d87-e053-2a95a90a1fc3	2019-12-09	Warnings	Exact identifier spl id: 994b65d2-4393-6d87-e053-2a95a90a1fc3 spl set id: 994b65d2-4392-6d87-e053-2a95a90a1fc3

Reported adverse events (FAERS/openFDA)#

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