Label: OSTEODORON AM BONE SUPPORT- pumpkin silicon dioxide calcium fluoride fluorapatite powder

  • 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 March 12, 2010

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  • Purpose

    Uses: For healthy teeth and bone development.

  • Dosage & Administration

    Directions: Take in the morning. Use with Osteodoron PM Bone Support Powder. Ages 12 and older:  1/8 tsp. Ages 2-11:  1/16 tsp. Under
    age 2: Ask a doctor.

  • OTC-Active Ingredient

    Active Ingredients: Cucurbita e flor. 3X HPUS, Apatite 6X HPUS, Fluorite 6X HPUS, Quartz 6X HPUS.

  • Inactive Ingredient

    Inactive Ingredient: Lactose

  • Keep out of reach of children

    KEEP OUT OF REACH OF CHILDREN.

  • Do not use section

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

  • Ask doctor section

    Consult your doctor if you are lactose intolerant, or if inadequate dietary calcium is a concern. When using this product, consult your doctor regularly to ensure that improvement is proceeding normally.

  • 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

    Osteodoron AM

    Bone Support Powder

    Homeopathic

    net vol. 60 ml (2 fl. oz.)

    osteodoron AM powder bottle label

  • INGREDIENTS AND APPEARANCE
    OSTEODORON AM BONE SUPPORT 
    pumpkin silicon dioxide calcium fluoride fluorapatite powder
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-7096
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PUMPKIN (UNII: SYW0QUB89Y) (PUMPKIN - UNII:SYW0QUB89Y) PUMPKIN3 [hp_X]
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE6 [hp_X]
    CALCIUM FLUORIDE (UNII: O3B55K4YKI) (CALCIUM FLUORIDE - UNII:O3B55K4YKI) CALCIUM FLUORIDE6 [hp_X]
    FLUORAPATITE (UNII: M4CM1H238J) (FLUORAPATITE - UNII:M4CM1H238J) FLUORAPATITE6 [hp_X]
    Inactive Ingredients
    Ingredient NameStrength
    LACTOSE (UNII: J2B2A4N98G)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48951-7096-41 in 1 BOTTLE, GLASS
    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
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