Label: 7030 CALCIUM PREMIUM- calcium capsule

  • Category: HUMAN OTC DRUG LABEL

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 March 17, 2021

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • ACTIVE INGREDIENT

    calcium

  • INACTIVE INGREDIENT

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

  • PURPOSE

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

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children

  • INDICATIONS & USAGE

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

  • WARNINGS

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

  • DOSAGE & ADMINISTRATION

    for oral use only

  • PRINCIPAL DISPLAY PANEL

    package insert
  • INGREDIENTS AND APPEARANCE
    7030 CALCIUM PREMIUM 
    calcium capsule
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55259-0002
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CALCIUM (UNII: SY7Q814VUP) (CALCIUM - UNII:SY7Q814VUP) CALCIUM0.99 
    Inactive Ingredients
    Ingredient NameStrength
    MAGNESIUM (UNII: I38ZP9992A)  
    ZINC OXIDE (UNII: SOI2LOH54Z)  
    SELENIUM (UNII: H6241UJ22B)  
    GERMANIUM (UNII: 00072J7XWS)  
    IRON (UNII: E1UOL152H7)  
    POTASSIUM (UNII: RWP5GA015D)  
    MANGANESE (UNII: 42Z2K6ZL8P)  
    Product Characteristics
    Colorwhite (white) Scoreno score
    ShapeOVAL (tablet) Size12mm
    FlavorImprint Code 3;hp;x
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55259-0002-1120 in 1 PACKAGE; Type 0: Not a Combination Product03/18/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other03/18/2021
    Labeler - Apexel Co., Ltd (687287979)
    Registrant - Apexel Co., Ltd (687287979)
    Establishment
    NameAddressID/FEIBusiness Operations
    Apexel Co., Ltd687287979manufacture(55259-0002)