CARTILAGO ARGENTUM cream

Cartilago Argentum by

Drug Labeling and Warnings

Cartilago Argentum by is a Homeopathic medication manufactured, distributed, or labeled by Uriel Pharmacy Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INDICATIONS & USAGE

Directions:FOR EXTERNAL USE ONLY.

DOSAGE & ADMINISTRATION

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

ACTIVE INGREDIENT

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

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

PURPOSE

Use: Temporary relief of joint pain.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN.

WARNINGS

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.

QUESTIONS

Questions? Call 866.642.2858
Made with care by Uriel, East Troy, WI 53120
www.urielpharmacy.com

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CARTILAGO ARGENTUM 
cartilago argentum cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 48951-3226
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BETULA PUBESCENS LEAF (UNII: 84SOH0O3OO) (BETULA PUBESCENS LEAF - UNII:84SOH0O3OO)	BETULA PUBESCENS LEAF	3 [hp_X]  in 1 g
ANTIMONY TRISULFIDE (UNII: F79059A38U) (ANTIMONY TRISULFIDE - UNII:F79059A38U)	ANTIMONY TRISULFIDE	5 [hp_X]  in 1 g
MANDRAGORA OFFICINARUM ROOT (UNII: I2XCB174VB) (MANDRAGORA OFFICINARUM ROOT - UNII:I2XCB174VB)	MANDRAGORA OFFICINARUM ROOT	3 [hp_X]  in 1 g
ACONITUM NAPELLUS (UNII: U0NQ8555JD) (ACONITUM NAPELLUS - UNII:U0NQ8555JD)	ACONITUM NAPELLUS	6 [hp_X]  in 1 g
ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW)	ARNICA MONTANA	6 [hp_X]  in 1 g
SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G)	SILVER	8 [hp_X]  in 1 g
BOS TAURUS CARTILAGE (UNII: UE77B10IIY) (BOS TAURUS CARTILAGE - UNII:UE77B10IIY)	BOS TAURUS CARTILAGE	6 [hp_X]  in 1 g

Inactive Ingredients
Ingredient Name	Strength
LAVENDER OIL (UNII: ZBP1YXW0H8)
CETYL ALCOHOL (UNII: 936JST6JCN)
POLYOXYL 40 STEARATE (UNII: 13A4J4NH9I)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
XANTHAN GUM (UNII: TTV12P4NEE)
TEA TREE OIL (UNII: VIF565UC2G)
CITRUS PARADISI SEED (UNII: 12F08874Y7)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
STEARIC ACID (UNII: 4ELV7Z65AP)
FRANKINCENSE OIL (UNII: 67ZYA5T02K)
WATER (UNII: 059QF0KO0R)
SORBIC ACID (UNII: X045WJ989B)
MYRRH OIL (UNII: H74221J5J4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 48951-3226-5	60 g in 1 TUBE; Type 0: Not a Combination Product	09/01/2009

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		09/01/2009

Labeler - Uriel Pharmacy Inc. (043471163)

Establishment
Name	Address	ID/FEI	Business Operations
Uriel Pharmacy Inc.		043471163	manufacture(48951-3226)