Stibium 6X

Manufacturer: Uriel Pharmacy Inc.
Effective date: 2025-01-20
Label type: HUMAN OTC DRUG LABEL
Version: 5
Source: full-release
Hydrated at: 2026-06-01 02:31:29

Label at a glance#

ProductStibium 6X

Active ingredientANTIMONY

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. 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: Stibium met. 6X

INACTIVE INGREDIENT SECTION

Inactive Ingredient: 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 Uriel, East Troy, WI 53120 shopuriel.com Lot:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Stibium 6X Powder

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-8401-4	Stibium 6X	50 g in 1 BOTTLE, GLASS	POWDER	50		5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-8401	STIBIUM 6X POWDER [URIEL PHARMACY INC.]	5	Current NDC, 1 package rows	20250121_0a1f3d5d-13d5-97b3-e063-6394a90aa250.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

Stibium 6X
LACTOSE
ANTIMONY

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
48951-8401	48951-8401-4

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	J2B2A4N98G	IACT
ANTIMONY	9IT35J3UV3	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
Stibium 6X	STIBIUM 6X	Uriel Pharmacy Inc.	0a1f3d5d-13d5-97b3-e063-6394a90aa250	2025-01-20	Warnings	Exact identifier ndc (package): 48951-8401-4 ndc (product): 48951-8401 ndc11 (package): 48951840104 spl id: 2c286b32-d8b5-9c06-e063-6394a90a3fbc spl set id: 0a1f3d5d-13d5-97b3-e063-6394a90aa250

Reported adverse events (FAERS/openFDA)#

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