ECHINACEA QUARTZ GUM SUPPORT GEL [URIEL PHARMACY INC.]

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ECHINACEA QUARTZ GUM SUPPORT GEL [URIEL PHARMACY INC.]
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NDC 48951-4019-5
Set ID 73cfeb15-0634-4f45-8561-8ed04c63b038
Category HUMAN OTC DRUG LABEL
Packager Uriel Pharmacy Inc.
Generic Name
Product Class
Product Number
Application Number
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  • INDICATIONS & USAGE

  • DOSAGE & ADMINISTRATION

    Directions: Apply to gums and inside of mouth as needed.

  • ACTIVE INGREDIENT

    Active Ingredients: 100 gm contains: 89 gm Althaea e rad. 2X; Echinacea e pl. tota 2X, Antimonite 5X, Argentum nitricum 20X, Atropa belladonna e pl. tota 20X, Quartz 20X

  • INACTIVE INGREDIENT

    Inactive Ingredients: Distilled water, Glycerin, Sodium alginate, Potassium sorbate, Chlorophyll, Stevioside, Rose oil, Grapefruit seed extract

  • 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: 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 www.urielpharmacy.com

  • PRINCIPAL DISPLAY PANEL

    product label

  • INGREDIENTS AND APPEARANCE
    ECHINACEA QUARTZ GUM SUPPORT 
    echinacea quartz gum support gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-4019
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALTHAEA OFFICINALIS ROOT (UNII: TRW2FUF47H) (ALTHAEA OFFICINALIS ROOT - UNII:TRW2FUF47H) ALTHAEA OFFICINALIS ROOT2 [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
    SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G) SILVER20 [hp_X]  in 1 g
    ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H) ATROPA BELLADONNA20 [hp_X]  in 1 g
    COLLOIDAL SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (COLLOIDAL SILICON DIOXIDE - UNII:ETJ7Z6XBU4) COLLOIDAL SILICON DIOXIDE20 [hp_X]  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM ALGINATE (UNII: C269C4G2ZQ)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    CHLOROPHYLL (UNII: 00WNZ48OR9)  
    STEVIOSIDE (UNII: 0YON5MXJ9P)  
    ROSE OIL (UNII: WUB68Y35M7)  
    CITRUS PARADISI SEED (UNII: 12F08874Y7)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48951-4019-560 g in 1 TUBE
    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(48951-4019)
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