Label: LEVISTICUM QUERCUS liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved homeopathic

DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

Drug Label Information

Updated November 28, 2023

If you are a consumer or patient please visit this version.

  • INDICATIONS & USAGE

    Directions: FOR ORAL USE.

  • DOSAGE & ADMINISTRATION

    Take 3-4 times daily. Ages 12 and older: 10 drops. Ages 2-11: 5 drops. Under age 2: Consult a doctor.

  • ACTIVE INGREDIENT

    Active Ingredients: Levisticum (Lovage) 6X, Quercus Cinis (Oak bark ash) 6X, Quercus (cort.) (Decoction of oak bark) 6X, Cornea (Bovine Cornea of the eye) 8X, Corpus vitreum (Bovine vitreous body of the eye) 8X, Lens cristallina (Bovine crystalline lens of the eye) 8X, Nervus opticus (Bovine second cranial nerve) 8X

  • INACTIVE INGREDIENT

    Inactive Ingredients: Water, Salt, Boric acid, Sodium bicarbonate, Rose oil

  • PURPOSE

    Use: Temporary relief of skin rash.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN.

  • WARNINGS

    Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. 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.

    REFRIGERATE AFTER OPENING. USE WITHIN 30 DAYS OF OPENING.
    Opened on:_________________

  • QUESTIONS

    Questions? Call 866.642.2858
    Made by Uriel, East Troy, WI 53120
    shopuriel.com

  • PRINCIPAL DISPLAY PANEL

    Levisticum Quercus Liquid 10mlLevisticum Quercus Liquid

  • INGREDIENTS AND APPEARANCE
    LEVISTICUM QUERCUS 
    levisticum quercus liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-6077
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BOS TAURUS PARASYMPATHETIC NERVE (UNII: WIE1G5542P) (BOS TAURUS PARASYMPATHETIC NERVE - UNII:WIE1G5542P) BOS TAURUS PARASYMPATHETIC NERVE8 [hp_X]  in 1 mL
    QUERCUS ROBUR WHOLE (UNII: R7QMG0BT2W) (QUERCUS ROBUR WHOLE - UNII:R7QMG0BT2W) QUERCUS ROBUR WHOLE6 [hp_X]  in 1 mL
    LEVISTICUM OFFICINALE ROOT (UNII: 46QZ19OEX8) (LEVISTICUM OFFICINALE ROOT - UNII:46QZ19OEX8) LEVISTICUM OFFICINALE ROOT6 [hp_X]  in 1 mL
    BOS TAURUS NERVE (UNII: 28G2U3MQJK) (BOS TAURUS NERVE - UNII:28G2U3MQJK) BOS TAURUS NERVE8 [hp_X]  in 1 mL
    BOS TAURUS EYE (UNII: VTW461N43P) (BOS TAURUS EYE - UNII:VTW461N43P) BOS TAURUS EYE8 [hp_X]  in 1 mL
    QUERCUS ALBA BARK (UNII: 93LP7Y8EGT) (QUERCUS ALBA BARK - UNII:93LP7Y8EGT) QUERCUS ALBA BARK6 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    BORIC ACID (UNII: R57ZHV85D4)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    ROSE OIL (UNII: WUB68Y35M7)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48951-6077-11 in 1 BAG09/01/2009
    110 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic09/01/2009
    Labeler - Uriel Pharmacy Inc. (043471163)
    Establishment
    NameAddressID/FEIBusiness Operations
    Uriel Pharmacy Inc.043471163manufacture(48951-6077)