FDA.reportPublic FDA data

Cartilago Argentum

Manufacturer
Uriel Pharmacy Inc.
Effective date
2018-11-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:47:02

Label at a glance#

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

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions:FOR EXTERNAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

Apply to joint(s) several times daily or as needed. Under age 2: Consult a doctor.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Betula (Silver birch leaves) 3X, Mandragora off. (Mandrake) 3X, Antimonite (Nat. antimony trisulfide) 5X, Aconitum (Monkshood) 6X, Arnica 6X, Argentum met. (Silver) 8X, Cartilago articularis (Bovine cartilage - knee joint) 8X

INACTIVE INGREDIENT SECTION

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

OTC - PURPOSE SECTION

Use: Temporary relief of joint pain.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

WARNINGS SECTION

Warnings: FOR EXTERNAL USE ONLY.
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, if conditions worsen or persist, or accidental ingestion occurs. 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
www.urielpharmacy.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Cartilago Argentum CreamCartilago Argentum Cream

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-322648951-3226-5

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Name, UNII, Kind table
NameUNIIKind
BETULA PUBESCENS LEAF84SOH0O3OOACTIB
ANTIMONY TRISULFIDEF79059A38UACTIB
LAVENDER OILZBP1YXW0H8IACT
CETYL ALCOHOL936JST6JCNIACT
POLYOXYL 40 STEARATE13A4J4NH9IIACT
STEARYL ALCOHOL2KR89I4H1YIACT
XANTHAN GUMTTV12P4NEEIACT
TEA TREE OILVIF565UC2GIACT
CITRUS PARADISI SEED12F08874Y7IACT
MANDRAGORA OFFICINARUM ROOTI2XCB174VBACTIB
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
ACONITUM NAPELLUSU0NQ8555JDACTIB
ARNICA MONTANAO80TY208ZWACTIB
SILVER3M4G523W1GACTIB
STEARIC ACID4ELV7Z65APIACT
FRANKINCENSE OIL67ZYA5T02KIACT
BOS TAURUS CARTILAGEUE77B10IIYACTIB
WATER059QF0KO0RIACT
SORBIC ACIDX045WJ989BIACT
MYRRH OILH74221J5J4IACT

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
0f3c8922-ed7a-d74c-e063-6394a90acf967acca117-84c0-251d-e053-2a91aa0a45462024-01-18WarningsExact identifier
spl set id: 7acca117-84c0-251d-e053-2a91aa0a4546

Reported adverse events (FAERS/openFDA)#

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