Label: BERBERIS OXALIS pellet

  • 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 December 2, 2024

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

  • INDICATIONS & USAGE

    Directions: FOR ORAL USE ONLY.

  • 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.

  • ACTIVE INGREDIENT

    Active Ingredients: Berberis (Barberry) 1X,Oxalis (Wood sorrel) 3X, Sabal serr. (Dwarf palm) 3X, Urtica urens (Small nettle) 3X, Viscum Abietis (Fir tree mistletoe) 4X, Mag. sulf. (Magnesium sulfate) 6X, Prostata (Bovine prostate gland) 8X,Ferrum picrinicum 8X,Granite (Primitive rock containing quartz, feldspar, mica) 10X

  • INACTIVE INGREDIENT

    Inactive Ingredients: Organic sucrose, Lactose.

    Prepared using rhythmical processes.

  • PURPOSE

    Use: Temporary relief of headache.

  • 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. Contains sugar. Diabetics and persons intolerant of sucrose (sugar): Consult a doctor before use. Do not use if allergic to any ingredient. Contains traces of lactose. 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

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

  • PRINCIPAL DISPLAY PANEL

    Berberis Oxalis Pellets

  • INGREDIENTS AND APPEARANCE
    BERBERIS OXALIS 
    berberis oxalis pellet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-2117
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    FERROUS PICRATE (UNII: 4WC457HQ10) (FERROUS PICRATE - UNII:4WC457HQ10) FERROUS PICRATE8 [hp_X]
    BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (BERBERIS VULGARIS ROOT BARK - UNII:1TH8Q20J0U) BERBERIS VULGARIS ROOT BARK1 [hp_X]
    OXALIS STRICTA WHOLE (UNII: 3STW243384) (OXALIS STRICTA WHOLE - UNII:3STW243384) OXALIS STRICTA WHOLE3 [hp_X]
    SAW PALMETTO (UNII: J7WWH9M8QS) (SAW PALMETTO - UNII:J7WWH9M8QS) SAW PALMETTO3 [hp_X]
    URTICA URENS (UNII: IHN2NQ5OF9) (URTICA URENS - UNII:IHN2NQ5OF9) URTICA URENS3 [hp_X]
    VISCUM ALBUM FRUITING TOP (UNII: BK9092J5MP) (VISCUM ALBUM FRUITING TOP - UNII:BK9092J5MP) VISCUM ALBUM FRUITING TOP4 [hp_X]
    MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM SULFATE, UNSPECIFIED6 [hp_X]
    BOS TAURUS PROSTATE GLAND (UNII: 1P66FXU2MW) (BOS TAURUS PROSTATE GLAND - UNII:1P66FXU2MW) BOS TAURUS PROSTATE GLAND8 [hp_X]
    PENOXSULAM (UNII: 784ELC1SCZ) (PENOXSULAM - UNII:784ELC1SCZ) PENOXSULAM10 [hp_X]
    Inactive Ingredients
    Ingredient NameStrength
    LACTOSE (UNII: J2B2A4N98G)  
    SUCROSE (UNII: C151H8M554)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize3mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48951-2117-21350 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product09/01/2009
    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(48951-2117)