Argentite 6X

Manufacturer: Uriel Pharmacy, Inc.
Effective date: 2024-11-11
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:28:53

Label at a glance#

ProductArgentite 6X

Active ingredientSILVER SULFIDE

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: Argentite (Cubic silver sulfide) 6x

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Argentite 6X Powder

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
6cca4355-1206-91f7-02de-17eef38a8622	Product name	1	20140508
751c581a-bf64-2fd7-b3ec-ca02c83e4a00	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
48951-1376-4	2026-01-29	C162847	48780-1	49896155-a254-586f-e063-e6dba90add90	Argentite 6X

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-1376-4	Argentite 6X	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
48951-1376	ARGENTITE 6X POWDER [URIEL PHARMACY, INC.]	1	1 package rows	20241114_26a8657a-672d-2603-e063-6394a90a7ca8.zip

Products#

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

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

Argentite 6X
SILVER SULFIDE
SILVER CATION
LACTOSE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
48951-1376	48951-1376-4

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
SILVER SULFIDE	9ZB10YHC1C	ACTIB
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
26a8657a-672e-2603-e063-6394a90a7ca8			26a8657a-672d-2603-e063-6394a90a7ca8	2024-11-11	Warnings	Exact identifier spl id: 26a8657a-672e-2603-e063-6394a90a7ca8 spl set id: 26a8657a-672d-2603-e063-6394a90a7ca8

Reported adverse events (FAERS/openFDA)#

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