Label: LEMON QUINCE 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 December 12, 2024

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  • INDICATIONS & USAGE

    Directions: ONLY FOR USE AS A NASAL SPRAY.

  • DOSAGE & ADMINISTRATION

    Ages 12 and older: 2-3 sprays. Ages 2-11: 1-2 sprays. Under age 2: Consult a doctor.

  • ACTIVE INGREDIENT

    Active Ingredients: Citrus (Lemon) 2X, Cydonia (Quince) 2X, Berberis (Barberry) 3X, Quartz (Rock crystal) 20X

  • INACTIVE INGREDIENT

    Inactive Ingredients: Distilled water, Aloe vera juice, Sodium chloride, Grapefruit seed extract

    Prepared using rhythmical processes.

  • PURPOSE

    Use: Temporary relief of nasal congestion and allergy symptoms.

  • 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. Do not use if safety seals on box are broken or missing.

    SHAKE WELL BEFORE USE.
    REFRIGERATE AFTER OPENING.
    USE WITHIN 30 DAYS OF OPENING.

  • QUESTIONS

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

  • PRINCIPAL DISPLAY PANEL

    Lemon Quince

  • INGREDIENTS AND APPEARANCE
    LEMON QUINCE 
    lemon quince spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-6086
    Route of AdministrationNASAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LEMON JUICE (UNII: AGN709ANTJ) (LEMON JUICE - UNII:AGN709ANTJ) LEMON JUICE2 [hp_X]  in 1 mL
    QUINCE (UNII: 12MCS4H09N) (QUINCE - UNII:12MCS4H09N) QUINCE2 [hp_X]  in 1 mL
    BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (BERBERIS VULGARIS ROOT BARK - UNII:1TH8Q20J0U) BERBERIS VULGARIS ROOT BARK3 [hp_X]  in 1 mL
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE20 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    CITRUS PARADISI SEED (UNII: 12F08874Y7)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48951-6086-130 mL 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 Inc.043471163manufacture(48951-6086)
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