FDA.reportPublic FDA data

Stannum 5X

Manufacturer
Uriel Pharmacy Inc.
Effective date
2025-01-22
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:31:31

Label at a glance#

ProductStannum 5X
Active ingredientTIN
Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR TOPICAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

Apply to skin as needed. Under age 2: Consult a doctor.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Stannum met. (Metallic tin) 5X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Distilled water, Stearic acid, Isopropyl myristate, Lavender oil, Cetyl alcohol, Polyoxyl 40 stearate, Stearyl alcohol, Xanthan gum, Frankincense oil, Myrrh oil, Sorbic acid, Tea tree oil, Grapefruit seed extract

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. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Avoid contact with eyes. 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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Stannum 5X CreamStannum 5X Cream

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-8351-5Stannum 5X60 g in 1 TUBECREAM602

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-8351STANNUM 5X CREAM [URIEL PHARMACY INC.]2Current NDC, Legacy NDC, 1 package rows20250124_7a8e2137-c840-37f9-e053-2991aa0ace59.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-835148951-8351-5

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
FRANKINCENSE OIL67ZYA5T02KIACT
SORBIC ACIDX045WJ989BIACT
LAVENDER OILZBP1YXW0H8IACT
STEARYL ALCOHOL2KR89I4H1YIACT
XANTHAN GUMTTV12P4NEEIACT
CITRUS PARADISI SEED12F08874Y7IACT
TEA TREE OILVIF565UC2GIACT
CETYL ALCOHOL936JST6JCNIACT
WATER059QF0KO0RIACT
STEARIC ACID4ELV7Z65APIACT
POLYOXYL 40 STEARATE13A4J4NH9IIACT
MYRRH OILH74221J5J4IACT
TIN387GMG9FH5ACTIB
ISOPROPYL MYRISTATE0RE8K4LNJSIACT

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Stannum 5XSTANNUM 5XUriel Pharmacy Inc.7a8e2137-c840-37f9-e053-2991aa0ace592025-01-22WarningsExact identifier
ndc (package): 48951-8351-5
ndc (product): 48951-8351
ndc11 (package): 48951835105
spl id: 2c52d67b-abff-a2fa-e063-6294a90a7882
spl set id: 7a8e2137-c840-37f9-e053-2991aa0ace59

Reported adverse events (FAERS/openFDA)#

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