Label: NICOMIDE- niacinamide, zinc glycinate, folic acid, cupric oxide, selenium and chromium tablet

  • NDC Code(s): 75854-343-60
  • Packager: Avion Pharmaceuticals, LLC
  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated October 11, 2023

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  • STATEMENT OF IDENTITY

    Rx Only Dietary Supplement

    DESCRIPTION

    Nicomide® Tablets is a prescription dietary supplement for oral administration, specifically formulated for the dietary management of patients with unique nutritional needs who require increased levels of one or more of the ingredients in this product. Each white-colored, oval-shaped tablet is debossed with 342 on one side and blank on the other.

    Supplement Facts
    Serving Size: 1 Tablet 
    Amount per serving: % Daily Value
     Niacinamide  750 mg† 
     Zinc (as Zinc Bisglycinate Chelate)* 27 mg180%
     Folate (as (6S)-N5-Methyltetrahydrofolic Acid Calcium Salt) 500 mcg125% 
     Copper (as Cupric Oxide)100% 
     Selenium (Selenium Amino Acid Chelate) 71% 
     Chromium (Chromium Amino Acid Chelate) 83%
      † Daily Value (DV) not established.

    OTHER INGREDIENTS

    Methocel K, Lactose Anhydrous, Silicon Dioxide, Stearic Acid, Microcrystalline Cellulose, Magnesium Stearate, Hydroxypropyl Methylcellulose, Triacetin, and Titanium Dioxide.

    INDICATIONS

    Nicomide® Tablets is indicated for use as a dietary supplement for patients who are deficient in, or who are at risk for deficiency in one or more of the ingredients in this product.

    CONTRAINDICATIONS

    This product is contraindicated in patients with a known hypersensitivity to any of the ingredients.

  • PRECAUTIONS

    PRECAUTIONS

    Large doses of Nicomide® Tablets should be administered with caution in patients with a history of jaundice, liver disease, or diabetes. Patients with chronic liver failure and/or renal failure should exercise extreme caution in taking prescribed supplements containing copper.

    Folic acid alone is improper treatment of pernicious anemia and other megaloblastic anemias where vitamin B12 is deficient. Folic acid especially in doses above 1.0 mg daily may obscure pernicious anemia in that hematologic remission may occur while neurological manifestations remain progressive.

    THESE STATEMENTS HAVE NOT BEEN EVALUATED BY THE FOOD AND DRUG ADMINISTRATION. THIS PRODUCT IS NOT INTENDED TO DIAGNOSE, TREAT, CURE, OR PREVENT ANY DISEASE.

    KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN.

  • WARNINGS

    WARNINGS

    If you are pregnant, nursing, or taking medication, consult your doctor before use. Use only under the advice and supervision of a physician if you have a history of jaundice, liver disease or diabetes. Abnormal liver function tests have been reported in persons taking daily doses of 500 mg or more of niacinamide. Folate intake should not exceed 250% of the Daily Value (1,000 mcg).

    PREGNANCY & NURSING MOTHERS

    Nicomide® Tablets is not indicated for use as a prenatal/postnatal multivitamin for lactating and nonlactating mothers. Physicians and medical practitioners should administer Nicomide® Tablets with caution to patients who are pregnant, lactating and/or taking medication.

    ADVERSE REACTIONS
    Allergic sensitization has been reported rarely following oral and parental administration of Folate.

  • DOSAGE & ADMINISTRATION

    DOSAGE AND ADMINISTRATION

    Take 1-2 tablets daily, as a dietary supplement, as directed by your physician.

    HOW SUPPLIED

    Nicomide® Tablets are white-colored, oval-shaped tablets debossed on one side with “342”, and are supplied in bottles of 60 tablets (75854-343-60). The listed product number is not a National Drug Code. Instead, Avion has assigned a product code formatted according to standard industry practice in order to comply with the formatting requirements of pharmacy and healthcare insurance computer systems.

    STORAGE

    Store at 20° - 25°C (68° - 77°F); excursions permitted to 15° - 30°C (59° - 86°F) [See USP Controlled Room Temperature.]

    MANUFACTURED FOR:
    Avion Pharmaceuticals, LLC
    Alpharetta, GA 30022
    1-888-61-AVION
    Rev. 1117-01

    *Subject to one or more claims of U.S. Patent Nos. 7,582,418, 7,838,042 and 8,425,956.

    Nicomide® is a registered trademark of Acella Pharmaceuticals, LLC. Under license from Acella Pharmaceuticals, LLC. All rights reserved.

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    75854-343-60

    Nicomide®

    Dietary Supplement

    60 Tablets
    Rx Only

    Avion
    PHARMACEUTICALS

    PRINCIPAL DISPLAY PANEL - 30 capsules
  • INGREDIENTS AND APPEARANCE
    NICOMIDE 
    niacinamide, zinc glycinate, folic acid, cupric oxide, selenium and chromium tablet
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:75854-343
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE750 mg
    ZINC GLYCINATE (UNII: 681VJX72FE) (ZINC CATION - UNII:13S1S8SF37) ZINC GLYCINATE27 mg
    FOLIC ACID (UNII: 935E97BOY8) (FOLIC ACID - UNII:935E97BOY8) FOLIC ACID500 ug
    CUPRIC OXIDE (UNII: V1XJQ704R4) (CUPRIC CATION - UNII:8CBV67279L) CUPRIC CATION2 mg
    SELENIUM (UNII: H6241UJ22B) (SELENIUM - UNII:H6241UJ22B) SELENIUM50 ug
    CHROMIUM (UNII: 0R0008Q3JB) (CHROMIUM - UNII:0R0008Q3JB) CHROMIUM100 ug
    Inactive Ingredients
    Ingredient NameStrength
    HYPROMELLOSE 2208 (100 MPA.S) (UNII: B1QE5P712K)  
    ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    TRIACETIN (UNII: XHX3C3X673)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    ColorWHITEScoreno score
    ShapeOVALSize23mm
    FlavorImprint Code 342
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75854-343-6060 in 1 BOTTLE; Type 0: Not a Combination Product12/08/2014
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other12/08/2014
    Labeler - Avion Pharmaceuticals, LLC (040348516)
    Registrant - Avion Pharmaceuticals, LLC (040348516)
    Establishment
    NameAddressID/FEIBusiness Operations
    Avion Pharmaceuticals, LLC040348516manufacture(75854-343)