Indications & Usage
Directions: FOR ORAL USE ONLY.
The following Structured Product Label (SPL) was submitted to the FDA by Uriel Pharmacy Inc for the product Berberis Larix (NDC 48951-2157). 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 ORAL USE ONLY.
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.
Active Ingredients: Achillea (Yarrow) 3X, Berberis (Barberry) 3X, Equisetum (Common horsetail) 3X, Cantharis (Spanish fly) 6X, Apis (Honeybee) 8X, Pyrite (Nat. Iron disulfide) 8X, Resina laricis (Larch resin) 8X, Vesica urinaria (Bovine urinary bladder) 8X
Inactive Ingredients: Organic sucrose, Lactose
Prepared using rhythmical processes.
Use: Temporary relief of bladder irritation.
KEEP OUT OF REACH OF CHILDREN.
Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Contains sugar. Diabetics and persons intolerant of sucrose (sugar): Consult a doctor before use. Contains traces of lactose. 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.
Questions? Call 866.642.2858
Uriel, East Troy, WI 53120
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