Supplement facts

Supplement Facts
Serving Size: 1 Tablet
Each Tablet Contains:
Niacinamide 750 mg
Zinc
(as Zinc bisglycinate chelate)
27 mg
Folate
(as L-methylfolate* calcium)
500 mcg
Copper
(as cupric oxide)
2 mg
Selenium
(Selenium amino acid chelate)
50 mcg
Chromium
(Chromium amino acid chelate)
100 mcg
* Nicomide® contains non-branded L-methylfolate vs. ingredients supplied by branded manufacturers. The L-methylfolate ((6S)-N5-methyltetrahydrofolic acid calcium salt) in Nicomide® is less than 1.0% D-isomer

Other Ingredients: Methocel K, Lactose Anhydrous, Silicon Dioxide, Stearic Acid, Microcrystalline Cellulose, Magnesium Stearate and Pharmaceutical Glaze (Dewaxed Bleached Shellac and Pure Ethyl Alcohol).

Dosage and administration:

Usual adult dose is one tablet taken twice daily, or as prescribed by physician.

Each Tablet Contains:

  • Niacinamide 750 mg
  • Zinc 27 mg
  • Folate 500 mcg 
  • Copper 2 mg
  • Selenium 50 mcg
  • Chromium 100 mcg

Precautions:

Large doses of Nicomide® should be administered with caution in patients with a history of jaundice, liver disease, or diabetes. Patients with chronic liver and / or renal failure should exercise extreme caution in taking prescribed supplements containing Copper. Abnormal liver function tests have been reported in persons taking a daily dose of 500mg or more of Niacinamide. Folic acid in doses above 1.0mg daily may obscure pernicious anemia in that hematologic remission can occur while neurological manifestations remain progressive. Folic acid intake should not exceed 250% of the recommended Daily Value (1.0mg), unless physician or healthcare provider explicitly prescribes otherwise.

Warnings:

Folic acid alone is improper treatment of pernicious anemia and other megaloblastic anemias where Vitamin B12 is deficient.

Pregnant Women & Nursing Mothers:

If you are pregnant, nursing or taking medication please consult with your physician or healthcare provider prior to using Nicomide®. Physicians should administer Nicomide® with extreme caution to patients who are pregnant, nursing or taking medication. Prior to prescribing Nicomide® (to pregnant women, nursing mothers or patients on medication), physicians and healthcare providers must consider the patient’s medical history and any drug(s), herb(s) and / or other medication consumption.

Minimal Side Effects:

  • Nausea has been reported when niacinamide and zinc were administered at dosages higher than recommended with Nicomide®; if experienced, administer with food.
  • Niacinamide is not associated with flushing, itching burning skin.
  • Allergic sensitization has been reported rarely following oral and parental administration of folic acid.
  • Although rare, transient elevations in liver function tests have been reported when niacinamide was administered at dosages greater than the recommended dose of Nicomide®.

Nicomide®. A supplement formulated with nutrients proven to help promote healthier overall skin.

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. CLICK HERE FOR IMPORTANT SAFETY INFORMATION.

Nicomide® contains non-branded L-methylfolate vs. ingredients supplied by branded manufacturers. The L-methylfolate ((6S)-N5-methyltetrahydrofolic acid calcium salt) in Nicomide® is less than 1.0% D-isomer.

*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.

Revision Designation: Rev. 0514

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