Label: GRAPHITE BELLADONNA liquid

  • Category: HUMAN OTC DRUG LABEL

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 October 25, 2021

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • INDICATIONS & USAGE

    Directions: FOR ORAL USE.

  • DOSAGE & ADMINISTRATION

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

  • ACTIVE INGREDIENT

    Active Ingredients: Helleborus (Christmas rose) 4X, Agaricus (Fly agaric mushroom) 6X, Argentite (Cubic silver sulfide) 6X,
    Regio substantia nigra (Bovine nucleus in the midbrain) 6X, Stannum met. (Metallic tin) 20X, Atropa belladonna (Nightshade) 30X,
    Graphite (Foliated crystalline carbon) 30X

  • INACTIVE INGREDIENT

    Inactive Ingredients: Water, Salt, Lactose

  • 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. 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.

  • QUESTIONS

    Questions? Call 866.642.2858
    Uriel, East Troy, WI 53120
    www.urielpharmacy.com Lot:

  • PRINCIPAL DISPLAY PANEL

    Graphite Belladonna Ampules

  • INGREDIENTS AND APPEARANCE
    GRAPHITE BELLADONNA 
    graphite belladonna liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-5126
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AMANITA MUSCARIA FRUITING BODY (UNII: DIF093I037) (AMANITA MUSCARIA FRUITING BODY - UNII:DIF093I037) AMANITA MUSCARIA FRUITING BODY6 [hp_X]  in 1 mL
    TIN (UNII: 387GMG9FH5) (TIN - UNII:387GMG9FH5) TIN20 [hp_X]  in 1 mL
    BOS TAURUS BRAIN (UNII: A1YEE2DB8Z) (BOS TAURUS BRAIN - UNII:A1YEE2DB8Z) BOS TAURUS BRAIN6 [hp_X]  in 1 mL
    HELLEBORUS NIGER ROOT (UNII: 608DGJ6815) (HELLEBORUS NIGER ROOT - UNII:608DGJ6815) HELLEBORUS NIGER ROOT4 [hp_X]  in 1 mL
    ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H) ATROPA BELLADONNA30 [hp_X]  in 1 mL
    GRAPHITE (UNII: 4QQN74LH4O) (GRAPHITE - UNII:4QQN74LH4O) GRAPHITE30 [hp_X]  in 1 mL
    SILVER SULFIDE (UNII: 9ZB10YHC1C) (SILVER CATION - UNII:57N7B0K90A) SILVER SULFIDE6 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48951-5126-110 in 1 BOX09/01/2009
    11 mL in 1 AMPULE; Type 1: Convenience Kit of Co-Package
    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(48951-5126)