Label: OSTEO-PORETICAL- calcium 600mg and vitamin d 1000iu tablet, film coated

  • NHRIC Code(s): 43063-907-14, 43063-907-60
  • Packager: PD-Rx Pharmaceuticals, Inc.
  • Category: DIETARY SUPPLEMENT
  • DEA Schedule: None
  • Marketing Status: Dietary Supplement

Drug Label Information

Updated September 21, 2021

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  • Supplement Facts

    Serving Size 1 Tablet

    Servings Per Container 60

    Amount Per Serving % Daily Value
    Vitamin D (as cholecalciferol) (1000 IU) 250%
    Calcium (as calcium carbonate) 600 mg 60%

    Other ingredients: cellulose, croscarmellose sodium, gum guar, magnesium stearate, ethylcellulose.

    * This statement has not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure or prevent disease.

  • DOSAGE & ADMINISTRATION

    For healthy adults, take one tablet twice daily, preferably with a meal. As a reminder, discuss this supplement and any medications you take with your health care providers. Intended for general use by adults in good health as recommended by their physician.

  • WARNINGS

    Do not take this supplement if pregnant nursing, have chronic kidney disease or kidney stones unless directed by your physicians. Not intended for use by infants or children. Discontinue use and consult your physician or poison control center if any adverse reactions or overdose occur. Keep out of reach of children. Do not use if tamper evident seal is broken.

  • SAFE HANDLING WARNING

    Store in a cool dry place protected from light.Keep bottle tightly closed.

  • PRINCIPAL DISPLAY PANEL

    For Bone & Colon Health*

    Physician & Pharmacist recommended

    Contains no sugar, lactose, salt or gluten

    Osteo-Poretical

    Calcium Supplement

    Calcium 600 mg + 1000 IU Vitamin D

    43063907 label

  • INGREDIENTS AND APPEARANCE
    OSTEO-PORETICAL 
    calcium 600mg and vitamin d 1000iu tablet, film coated
    Product Information
    Product TypeDIETARY SUPPLEMENTItem Code (Source)NHRIC:43063-907
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHOLECALCIFEROL (UNII: 1C6V77QF41) (CHOLECALCIFEROL - UNII:1C6V77QF41) CHOLECALCIFEROL1000 [iU]
    CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CATION600 mg
    Inactive Ingredients
    Ingredient NameStrength
    POWDERED CELLULOSE (UNII: SMD1X3XO9M)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    GUAR GUM (UNII: E89I1637KE)  
    ETHYLCELLULOSE, UNSPECIFIED (UNII: 7Z8S9VYZ4B)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NHRIC:43063-907-1414 in 1 BOTTLE, PLASTIC
    2NHRIC:43063-907-6060 in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    DIETARY SUPPLEMENT07/22/2019
    Supplement Facts
    Serving Size : Serving per Container :
    Amount Per Serving% Daily Value
    color
    scoring1
    shape
    size (solid drugs)19 mm
    Labeler - PD-Rx Pharmaceuticals, Inc. (156893695)
    Registrant - PD-Rx Pharmaceuticals, Inc. (156893695)
    Establishment
    NameAddressID/FEIBusiness Operations
    PD-Rx Pharmaceuticals, Inc.156893695repack(43063-907)
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