Label: QUERCETIN- quercetin liquid

  • NDC Code(s): 43742-0217-1
  • Packager: Deseret Biologicals, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved homeopathic

Drug Label Information

Updated 04/15

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  • ACTIVE INGREDIENTS:

    Quercetin 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C

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  • INDICATIONS:

    For temporary relief of symptoms related to food and pollen sensitivities including fatigue, headache, runny nose and congestion, itching eyes, diarrhea, bloating, and cramps. 

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  • WARNINGS:

    Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away.

    If pregnant or breast-feeding, ask a health professional before use.

    Tamper seal: "Sealed for Your Protection." Do not use if seal is broken or missing.

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  • DIRECTIONS:

    1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

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  • INACTIVE INGREDIENTS:

    Demineralized Water, 25% Ethanol.

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  • KEEP OUT OF REACH OF CHILDREN:

    Keep out of reach of children. In case of overdose, contact physician or Poison Control Center right away.

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  • INDICATIONS:

    For temporary relief of symptoms related to food and pollen sensitivities including fatigue, headache, runny nose and congestion, itching eyes, diarrhea, bloating, and cramps.

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  • QUESTIONS:

    Dist. By: Deseret Biologicals, Inc.

    469 W. Parkland Drive

    Sandy, UT 84070

    www.desbio.com

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  • PACKAGE LABEL DISPLAY:

    DESBIO

    NDC 43742-0217-1

    HOMEOPATHIC

    QUERCETIN

    1 FL OZ (30 ml)

    Quercetin

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  • INGREDIENTS AND APPEARANCE
    QUERCETIN 
    quercetin liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:43742-0217
    Route of Administration ORAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    QUERCETIN (UNII: 9IKM0I5T1E) (QUERCETIN - UNII:9IKM0I5T1E) QUERCETIN 6 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:43742-0217-1 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 04/11/2013
    Labeler - Deseret Biologicals, Inc. (940741853)
    Registrant - Apotheca Company (844330915)
    Establishment
    Name Address ID/FEI Business Operations
    Apotheca Company 844330915 manufacture(43742-0217) , api manufacture(43742-0217) , label(43742-0217) , pack(43742-0217)
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