Indications & Usage
Directions: FOR ORAL USE ONLY.
Cartilago Betula Pellet
FDA Label NDC 48951-3041
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 Betula (NDC 48951-3041). 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, warnings, otc - questions, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Dosage & Administration
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
Active Ingredients: Betula (Silver birch leaves) 5X, Aconitum (Monkshood) 6X, Arnica 6X, Cartilago articularis (Bovine cartilage - knee joint) 8X, Stannum (Metallic tin) 8X, Aurum (Metallic gold) 10X, Allium cepa e bulbo (Onion) 17X, Formica ex animale (Red wood ant) 17X
Inactive Ingredient
Inactive Ingredient: Sucrose
Otc - Purpose
Use: Temporary relief of sore muscles.
Warnings
Warnings: Contains sugar. Diabetics
and persons intolerant of sucrose (sugar): Consult a doctor before use. Do not use if allergic to any ingredient. Consult a doctor before use 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. Natural ingredients may cause color, scent and/or taste variation.
Otc - Questions
Questions? Call 866.642.2858
Uriel, East Troy, WI 53120
www.urielpharmacy.com
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