Stannum 21X

Manufacturer: Uriel Pharmacy Inc.
Effective date: 2026-01-16
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 02:36:49

Label at a glance#

ProductStannum 21X

Active ingredientTIN

Label structure9 sections

Contacts and useful links#

PhoneLabel contact866.642.2858

Label contents#

Full prescribing information#

OTC - PURPOSE SECTION

Use: Temporary relief of headache.

INDICATIONS & USAGE SECTION

FOR ORAL USE ONLY

DOSAGE & ADMINISTRATION SECTION

Directions: Take the contents of one ampule under the tongue and hold for 30 seconds, then swallow. Follow inside instructions to open ampule.

WARNINGS SECTION

Warnings:
NOT FOR INJECTION
Do not use if allergic to any ingredient. Consult a physician if symptoms worsen. If pregnant or nursing, consult a physician before use.
Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Stannum metallicum (Metallic tin) 21X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, Salt

Prepared using rythmical processes.

OTC - QUESTIONS SECTION

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

Lot:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Stannum 21X Ampule

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
48951-8361-1	2026-01-16	C162847	48780-1	2cef2736-8c80-d83d-e063-dadaa90ab31f	Stannum 21X
48951-8361-1	2025-01-30	C162847	48780-1	2cef2736-8c80-d83d-e063-dadaa90ab31f	Stannum 21X

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-8361-1	Stannum 21X	1 mL in 1 AMPULE	LIQUID	1		2
48951-8361-1	Stannum 21X	10 in 1 BOX	LIQUID	10		2

Products#

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

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

Stannum 21X
TIN
WATER
SODIUM CHLORIDE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
48951-8361	48951-8361-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
TIN	387GMG9FH5	ACTIB
WATER	059QF0KO0R	IACT
SODIUM CHLORIDE	451W47IQ8X	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
Stannum 21X	STANNUM 21X	Uriel Pharmacy Inc.	969cb4b7-c1c2-0577-e053-2a95a90a4e2c	2026-01-16	Warnings	Exact identifier ndc (package): 48951-8361-1 ndc (product): 48951-8361 ndc11 (package): 48951836101 spl id: 4886865e-c543-7b22-e063-6394a90a6f14 spl set id: 969cb4b7-c1c2-0577-e053-2a95a90a4e2c

Reported adverse events (FAERS/openFDA)#

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