Label: 7030 CALCIUM GOLD- calcium capsule

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated February 1, 2015

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  • ACTIVE INGREDIENT

    calcium

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  • INACTIVE INGREDIENT

    magnesium, zinc oxide, selenium, germanium, iron, potassium, manganese

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  • PURPOSE

    - to prevent and cure the osteoporosis
    - to prevent and cure the disease of cardiac and vascular
    - to promote growth and healing

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  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children

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  • INDICATIONS & USAGE

    take two tablets everty time, two times a day with enough water

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  • WARNINGS

    • Do not use during pregnant, breast-feeding, or menstrual cycle
    • Keep this product out of reach of children under 3 years old

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  • DOSAGE & ADMINISTRATION

    for oral use only

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  • INGREDIENTS AND APPEARANCE
    7030 CALCIUM GOLD 
    calcium capsule
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:55259-1001
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CALCIUM (UNII: SY7Q814VUP) (CALCIUM - UNII:SY7Q814VUP) CALCIUM 0.99 
    Inactive Ingredients
    Ingredient Name Strength
    MAGNESIUM (UNII: I38ZP9992A)  
    ZINC OXIDE (UNII: SOI2LOH54Z)  
    SELENIUM (UNII: H6241UJ22B)  
    GERMANIUM (UNII: 00072J7XWS)  
    IRON (UNII: E1UOL152H7)  
    POTASSIUM (UNII: RWP5GA015D)  
    MANGANESE (UNII: 42Z2K6ZL8P)  
    Product Characteristics
    Color white (white) Score no score
    Shape OVAL (tablet) Size 12mm
    Flavor Imprint Code 3;hp;x
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:55259-1001-1 120 in 1 PACKAGE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved drug other 03/10/2013
    Labeler - Apexel Co., Ltd (687287979)
    Registrant - Apexel Co., Ltd (687287979)
    Establishment
    Name Address ID/FEI Business Operations
    Apexel Co., Ltd 687287979 manufacture(55259-1001)
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