Indications & Usage
Directions: FOR ORAL USE.
Cartilago Argentum
FDA Label NDC 48951-3261
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Uriel Pharmacy Inc. for the product Cartilago Argentum (NDC 48951-3261). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding indications & usage, dosage & administration, otc - active ingredient, inactive ingredient, otc - purpose, otc - keep out of reach of children, warnings, otc - questions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Dosage & Administration
Take the contents of one ampule under the tongue and hold for 30 seconds, then swallow.
Otc - Active Ingredient
Active Ingredients: Mandragora (Mandrake) 5X, Aconitum (Monkshood) 6X, Antimonite (Nat. antimony trisulfide) 6X, Arnica 6X, Betula (Silver birch leaves) 6X, Argentum met. (Silver) 8X, Cartilago articularis (Bovine cartilage - hip joint/knee joint) 8X
Inactive Ingredient
Inactive Ingredients: Water, Salt, Lactose
"prepared using rhythmical processes"
Otc - Purpose
Use: Temporary relief of aches and pains in the joints.
Otc - Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN.
Warnings
Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Contains traces of lactose. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use.
Otc - Questions
Questions? Call 866.642.2858 Uriel, East Troy, WI 53120 shopuriel.com
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