Label: ZINC SULFATE tablet

  • NDC Code(s): 42937-807-10
  • Packager: NATIONWIDE LABORATORIES, LLC
  • Category: DIETARY SUPPLEMENT
  • DEA Schedule: None
  • Marketing Status: Dietary Supplement

Drug Label Information

Updated April 19, 2016

If you are a consumer or patient please visit this version.

  • DOSAGE & ADMINISTRATION

    Supplement Facts
    Serving Size: 1 Tablet
    Servings Per Container: 100
    Amount per Serving% Daily Value*
    Zinc Sulfate (yielding 50 mg of Zinc )220 mg333% **

    * Based on a 2,000 calorie diet

    ** Daily Values not established

  • OTHER INGREDIENTS:

    Calcium Carbonate, Dicalcium Phosphate, Microcrystalline Cellulose, Magnesium Stearate, Stearic Acid, Starch, Crosscarmallose Sodium, Silicon dioxide and Pharmaceutical Glaze.

  • DESCRIPTION:

    ZINC SULFATE Tablets is an orally administered dietary supplement and should be administered under the supervision of a licensed medical practitioner.

    Supplied as a round white to off white colored tablets dispensed in bottle of 100 tablets.

  • DOSAGE:

    1 to 2 tablet(s) daily or as directed by a physician.

  • WARNING:

    KEEP THIS AND ALL MEDICATION OUT OF REACH OF CHILDREN.

  • CAUTION:

    Seek medical attention right away if any SEVERE side effects occur:

  • STORAGE:

    Store at Room Temperature 15°-30°C (59°-86°F).

    Call your licensed medical practitioner about this product.

    Manufactured for:
    Nationwide Laboratories, LLC.
    Iselin, New Jersey 08830

  • PRINCIPAL DISPLAY PANEL

    NDC 42937-807-10

    ZINC SULFATE

    TABLETS

    220 mg

    DIETARY SUPPLEMENT

    To treat and prevent zinc deficiency.

    100 Tablets

    image description

  • INGREDIENTS AND APPEARANCE
    ZINC SULFATE 
    zinc sulfate tablet
    Product Information
    Product TypeDIETARY SUPPLEMENTItem Code (Source)NHRIC:42937-807
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC SULFATE (UNII: 89DS0H96TB) (ZINC CATION - UNII:13S1S8SF37) ZINC SULFATE220 mg
    Inactive Ingredients
    Ingredient NameStrength
    CALCIUM CARBONATE (UNII: H0G9379FGK)  
    DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NHRIC:42937-807-10100 in 1 BOTTLE, DISPENSING
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    dietary supplement04/22/2016
    Supplement Facts
    Serving Size : Serving per Container :
    Amount Per Serving% Daily Value
    color
    shape
    size (solid drugs)11 mm
    scoring1
    Labeler - NATIONWIDE LABORATORIES, LLC (078366153)