Indications & Usage
Directions:FOR EXTERNAL USE ONLY.
The following Structured Product Label (SPL) was submitted to the FDA by Uriel Pharmacy Inc. for the product Cartilago Argentum (NDC 48951-3260). 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.
Directions:FOR EXTERNAL USE ONLY.
Apply to joint(s) several times daily or as needed. Under age 2: Consult a doctor.
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 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, Lactose
Use: Temporary relief of joint pain.
KEEP OUT OF REACH OF CHILDREN.
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. Contains traces of lactose. 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? Call 866.642.2858
Made with care by Uriel, East Troy, WI 53120
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