FDA.reportPublic FDA data

Cartilago Argentum

Manufacturer
Uriel Pharmacy Inc.
Effective date
2024-12-06
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:29:23

Label at a glance#

ProductCartilago Argentum
Active ingredientBETULA PUBESCENS BARK, SILVER, MANDRAGORA OFFICINARUM ROOT, ARNICA MONTANA FLOWER, ACONITUM NAPELLUS, ANTIMONY TRISULFIDE, BOS TAURUS CARTILAGE
Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR ORAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

Dissolve pellets under the tongue 3-4 times daily. Ages 12 and older: 10 pellets. Ages 2-11: 5 pellets. Under age 2: Consult a doctor.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Mandragora (Mandrake) 5X, Aconitum (Monkshood) 6X, Antimonite (Nat. antimony trisulfide) 6X, Arnica 6X, Betula (Silver birch leaves) 6X, Cartilago articularis (Bovine cartilage) 8X, Argentum metallicum (Silver) 8X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Organic sucrose, Lactose

Prepared using rhythmical processes.

OTC - PURPOSE SECTION

Use: Temporarily relieves aches and pains in joints.

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. Contains sugar. Diabetics and persons intolerant of sucrose (sugar): Consult a doctor before use. Do not use if allergic to any ingredient. Contains traces of lactose. Consult a doctor 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

Cartilago Argentum PelletsCartilago Argentum Pellets

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-3232-2Cartilago Argentum1350 in 1 BOTTLE, GLASSPELLET13504

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-3232CARTILAGO ARGENTUM PELLET [URIEL PHARMACY INC.]4Legacy NDC, 1 package rows20241208_969eefb2-a801-6374-e053-2a95a90ac464.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-323248951-3232-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
BETULA PUBESCENS BARK3R504894L9ACTIB
SILVER3M4G523W1GACTIB
SUCROSEC151H8M554IACT
MANDRAGORA OFFICINARUM ROOTI2XCB174VBACTIB
ARNICA MONTANA FLOWEROZ0E5Y15PZACTIB
LACTOSE, UNSPECIFIED FORMJ2B2A4N98GIACT
ACONITUM NAPELLUSU0NQ8555JDACTIB
ANTIMONY TRISULFIDEF79059A38UACTIB
BOS TAURUS CARTILAGEUE77B10IIYACTIB

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
289f67c0-7c90-0b37-e063-6394a90abd4d969eefb2-a801-6374-e053-2a95a90ac4642024-12-06WarningsExact identifier
spl id: 289f67c0-7c90-0b37-e063-6394a90abd4d
spl set id: 969eefb2-a801-6374-e053-2a95a90ac464

Reported adverse events (FAERS/openFDA)#

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