Label: ECHINACEA QUARTZ gel

  • 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 September 26, 2023

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  • INDICATIONS & USAGE

    Directions: FOR TOPICAL USE ONLY.

  • DOSAGE & ADMINISTRATION

    Apply to gums and inside of mouth as needed. Under age 2: Consult a doctor.

  • ACTIVE INGREDIENT

    Active Ingredients: 100 gm contains: 89 gm Althaea (Marsh mallow root) 2X; Echinacea (Purple coneflower) 2X, Antimonite (Nat. antimony trisulfide) 5X, Argentum nitricum (Silver nitrate) 20X, Atropa belladonna (Nightshade) 20X, Quartz (Rock crystal) 20X

  • INACTIVE INGREDIENT

    Inactive Ingredients: Distilled water, Boric acid, Glycerin, Sodium alginate, Sodium hydroxide, Sorbic acid, Tea tree oil, Chlorophyll, Stevioside, Grapefruit seed extract, Rose oil

  • PURPOSE

    Uses: Temporarily relieves symptoms of hypersensitive teeth, gum inflammation, soreness or dryness in the mouth and may be used before and after dental work.

  • 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. Avoid contact with eyes. Do not use if safety seal is broken or missing.

  • QUESTIONS

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

  • PRINCIPAL DISPLAY PANEL

    Echinacea Quartz Gel

  • INGREDIENTS AND APPEARANCE
    ECHINACEA QUARTZ 
    echinacea quartz gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-4172
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G) SILVER20 [hp_X]  in 1 g
    ECHINACEA, UNSPECIFIED (UNII: 4N9P6CC1DX) (ECHINACEA, UNSPECIFIED - UNII:4N9P6CC1DX) ECHINACEA, UNSPECIFIED2 [hp_X]  in 1 g
    ANTIMONY TRISULFIDE (UNII: F79059A38U) (ANTIMONY TRISULFIDE - UNII:F79059A38U) ANTIMONY TRISULFIDE5 [hp_X]  in 1 g
    ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H) ATROPA BELLADONNA20 [hp_X]  in 1 g
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE20 [hp_X]  in 1 g
    ALTHAEA OFFICINALIS ROOT (UNII: TRW2FUF47H) (ALTHAEA OFFICINALIS ROOT - UNII:TRW2FUF47H) ALTHAEA OFFICINALIS ROOT2 [hp_X]  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM ALGINATE (UNII: C269C4G2ZQ)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    SORBIC ACID (UNII: X045WJ989B)  
    CITRUS PARADISI SEED (UNII: 12F08874Y7)  
    STEVIOSIDE (UNII: 0YON5MXJ9P)  
    WATER (UNII: 059QF0KO0R)  
    BORIC ACID (UNII: R57ZHV85D4)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    ROSE OIL (UNII: WUB68Y35M7)  
    CHLOROPHYLL (UNII: 00WNZ48OR9)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48951-4172-560 g in 1 TUBE; Type 0: Not a Combination Product06/28/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic06/28/2022
    Labeler - Uriel Pharmacy, Inc. (043471163)
    Establishment
    NameAddressID/FEIBusiness Operations
    Uriel Pharmacy, Inc.043471163manufacture(48951-4172)
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