Label: PURPLE CONEFLOWER spray

  • 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 July 24, 2017

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  • Purpose

    Uses: Temporary relieves symptoms of sore throat and mouth inflammation.

  • Dosage & Administration


    Directions: Take up to every 1-2 hours as needed. Ages 12 and older: 2-3 sprays.  Ages 2-11: 1-2 sprays.  Under age 2: Ask a doctor.

  • OTC-Active Ingredient

    Active Ingredients: Calendula 1X, Echinacea (Purple coneflower) 1X, Eucalyptus 1X, Salvia (Sage) 1X, Gingiva (Bovine gums) 8X, Tonsilla (Bovine tonsil) 8X, Vaucheria (Fresh water algae) 8X, Argentum nitricum (Silver nitrate) 21X, Atropa belladonna (Nightshade) 21X, Quartz (Rock crystal) 21X

  • Uses: Temporary relieves symptoms of sore throat and mouth inflammation.

  • Inactive Ingredient

    Inactive Ingredients: Organic cane alcohol, Water, Eucalyptus oil, Gingiva, Tonsilla, Vaucheria.

  • Keep out of reach of children

    KEEP OUT OF REACH OF CHILDREN.

  • WARNINGS

    Do not use if allergic to any ingredient. Do not use if safety seal is broken or missing.

  • Ask doctor section

    Consult a doctor if symptoms worsen or persist.

  • Pregnancy or breast feeding section

    If you are pregnant or nursing, consult a doctor before use.

  • Questions section

    Questions? Uriel Pharmacy

    866 642-2858  East Troy, WI 53120 

    www.urielpharmacy.com

  • Principal Display Panel

    PurpleConeflowerSpray

  • INGREDIENTS AND APPEARANCE
    PURPLE CONEFLOWER 
    purple coneflower spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-8318
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SAGE (UNII: 065C5D077J) (SAGE - UNII:065C5D077J) SAGE1 [hp_X]
    CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (CALENDULA OFFICINALIS FLOWERING TOP - UNII:18E7415PXQ) CALENDULA OFFICINALIS FLOWERING TOP1 [hp_X]
    ECHINACEA PALLIDA (UNII: 904CK3270L) (ECHINACEA PALLIDA - UNII:904CK3270L) ECHINACEA PALLIDA1 [hp_X]
    EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6) (EUCALYPTUS GLOBULUS LEAF - UNII:S546YLW6E6) EUCALYPTUS GLOBULUS LEAF1 [hp_X]
    MERCURIC CYANIDE (UNII: RWG7BD1032) (MERCURIC CYANIDE - UNII:RWG7BD1032) MERCURIC CYANIDE8 [hp_X]
    SILVER NITRATE (UNII: 95IT3W8JZE) (SILVER CATION - UNII:57N7B0K90A) SILVER NITRATE20 [hp_X]
    ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H) ATROPA BELLADONNA20 [hp_X]
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE20 [hp_X]
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48951-8318-2360 in 1 BOTTLE, SPRAY; 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 Inc043471163manufacture(48951-8318)
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