Levico Prunus Liquid
FDA Label NDC 48951-6026

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 Levico Prunus (NDC 48951-6026). 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

Indications & Usage

Directions: FOR ORAL USE ONLY.

Dosage & Administration

Take the contents of one ampule under the tongue and hold for 30 seconds, then swallow.

Otc - Active Ingredient

Active Ingredients: Hypericum (St. John’s Wort) 3X, Levico water (Mineral spring water) 3X, Prunus spinosa cum Ferro (Blackthorn, Iron) 6X

Inactive Ingredient

Inactive Ingredients: Water, Salt

Otc - Purpose

Use: Temporary relief of fatigue.

Otc - Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN.

Warnings

Warnings: 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. 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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