Label: ARNICA SCORODITE 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 February 6, 2024

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  • 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: Amethyst (Nat. silicic acid anhydrate with traces of manganese and iron) 6X, Arnica 6X, Conchae (Oyster shells) 6X, Levisticum (Lovage) 6X, Natrium carb. (Sodium carbonate monohydrate) 6X, Orchis e tub. decoct. (Orchid) 6X, Apatite (Nat. calcium fluorophosphate) 7X, Scorodite (Nat. ferric arsenate) 7X, Cerebellum (Bovine cerebellum) 8X

  • INACTIVE INGREDIENT

    Inactive Ingredients: Water, Salt, 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. 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
    shopuriel.com Lot:

  • PRINCIPAL DISPLAY PANEL

    Arnica Scorodite Ampules

  • INGREDIENTS AND APPEARANCE
    ARNICA SCORODITE 
    arnica scorodite liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-1155
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE6 [hp_X]  in 1 mL
    ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW) ARNICA MONTANA6 [hp_X]  in 1 mL
    OSTREA EDULIS SHELL (UNII: 49OY13BE7Z) (OSTREA EDULIS SHELL - UNII:49OY13BE7Z) OSTREA EDULIS SHELL6 [hp_X]  in 1 mL
    LEVISTICUM OFFICINALE ROOT (UNII: 46QZ19OEX8) (LEVISTICUM OFFICINALE ROOT - UNII:46QZ19OEX8) LEVISTICUM OFFICINALE ROOT6 [hp_X]  in 1 mL
    SODIUM CARBONATE (UNII: 45P3261C7T) (CARBONATE ION - UNII:7UJQ5OPE7D) SODIUM CARBONATE6 [hp_X]  in 1 mL
    ORCHIS MASCULA TUBER (UNII: 5H2N55J61B) (ORCHIS MASCULA TUBER - UNII:5H2N55J61B) ORCHIS MASCULA TUBER6 [hp_X]  in 1 mL
    FLUORAPATITE (UNII: M4CM1H238J) (FLUORAPATITE - UNII:M4CM1H238J) FLUORAPATITE7 [hp_X]  in 1 mL
    FERROUS ARSENATE (UNII: 129CO35H12) (FERROUS ARSENATE - UNII:129CO35H12) FERROUS ARSENATE7 [hp_X]  in 1 mL
    BOS TAURUS CEREBELLUM (UNII: Q09851U44F) (BOS TAURUS CEREBELLUM - UNII:Q09851U44F) BOS TAURUS CEREBELLUM8 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48951-1155-110 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(48951-1155)
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