Indications & Usage
Directions: FOR ORAL USE ONLY.
Onopordon Comp.
FDA Label NDC 48951-7090
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 Onopordon Comp. (NDC 48951-7090). 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
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: 100gm contains: 25gm Onopordon (Cotton thistle) 1X, 25gm Primula (Cowslip) 1X, 25gm Hyoscyamus (Henbane) 4X
Inactive Ingredient
Inactive Ingredient: Organic sucrose
Otc - Purpose
Use: Promotes healthy circulatory support.
Otc - Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN.
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.
Otc - Questions
Questions? Call 866.642.2858
Uriel, East Troy WI 53120
www.urielpharmacy.com
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