Label: APATITE CUCURBITA powder

  • Category: HUMAN OTC DRUG LABEL

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 17, 2024

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  • INDICATIONS & USAGE

    Directions: FOR ORAL USE ONLY.

  • DOSAGE & ADMINISTRATION

    Take 3-4 times daily. Ages 12 and older: 1/8 teaspoon. Ages 2-11: 1/16 teaspoon. Under age 2: Consult a doctor.

  • ACTIVE INGREDIENT

    Active Ingredients: Cucurbita (Pumpkin) 3X, Apatite (Nat. calcium fluorophosphate) 6X

  • INACTIVE INGREDIENT

    Inactive Ingredient: Lactose

    Prepared using rhythmical processes.

  • PURPOSE

    Use: For healthy teeth and bone development.

  • 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. Contains lactose. 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 seal is broken or missing.

  • QUESTIONS

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

  • PRINCIPAL DISPLAY PANEL

    Apatite Cucurbita Powder

  • INGREDIENTS AND APPEARANCE
    APATITE CUCURBITA 
    apatite cucurbita powder
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-1386
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CUCURBITA PEPO FLOWER (UNII: 413MGP37HQ) (CUCURBITA PEPO FLOWER - UNII:413MGP37HQ) CUCURBITA PEPO FLOWER3 [hp_X]  in 1 g
    FLUORAPATITE (UNII: M4CM1H238J) (FLUORAPATITE - UNII:M4CM1H238J) FLUORAPATITE6 [hp_X]  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    LACTOSE (UNII: J2B2A4N98G)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48951-1386-450 g in 1 BOTTLE, GLASS; 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(48951-1386)
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