Generic Name: niacinamide, azelaic acid, zinc, pyridoxine, cupric oxide and folic acid
Dosage Form: tablet, coated
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.
Prescription Dietary Supplement
VP-ZEL tablets Description
VP-ZEL Tabs is an orally administered prescription dietary supplement specifically formulated for the dietary management of patients with unique nutritional needs requiring increased folate levels and nutritional supplementation.
VP-ZEL Tabs should be administered under the supervision of a licensed medical practitioner.
Each coated, purple colored, oval-shaped tablet contains the following dietary ingredients:
|Serving Size: 1 Pill||Servings Per Container: 60|
|Amount Per Serving||% Daily Value|
|Nicotinamide (Vitamin B3)||600 mg||*|
|Azelaic Acid†||5 mg||*|
|Zinc (Zinc Oxide)||10 mg||*|
|Pyridoxine (Vitamin B6)||5 mg||*|
|Copper (Cupric Oxide)||1.5 mg||*|
|Folic acid||500 mcg||*|
Other ingredients: Microcrystalline cellulose, dicalcium phosphate, croscarmellose sodium, stearic acid, magnesium stearate, silica, and film coat (polyvinyl alcohol, polyethylene glycol, titanium dioxide, talc, FD&C blue #1 lake, and FD&C red #3).
The term "folate" are B vitamins that include folic acid and any forms of active pteroylglutamates regardless of the reduction state of the molecule. Folates, or vitamin B9, are primarily hydrolyzed in the intestinal jejunum and the liver to the active circulating form of folate, l-methylfolate, with an intermediate stable form, 5,10-methylenetetrahydrofolate.
Individuals with genetic polymorphorisms for the genes coding methylenetetrahydrofolate reductase (MTHFR) may not be capable of utilizing or metabolizing folic acid adequately for the vitamin B12 dependent methylation cycle.
Folic acid, including reduced forms1 such as folinic acid, may obscure pernicious anemia above 0.1 mg doses, and must be administered under the supervision of a licensed medical practitioner.
The 1971, 1972, 1973, 1980, 1984, 2000, and 2010 Federal Register Notices addressed this concern while establishing that increased folate was proper therapy in megaloblastic anemias - specifically where homocysteine levels were elevated or risk of neural tube defects (NTDs) was at issue. The Federal Register Notice of August 2, 1973 (38 FR 20750) specifically states that:
- Dietary supplement preparations are available without a prescription (21 CFR 121.1134).
- Levels higher than dietary supplement amounts are available only with a prescription.
Folic acid - including reduced forms, may be added to medical foods as defined in section 5(b) (3) of the Orphan Drug Act (21 USC 360ee(b)(3)), or to food (21 CFR 172.345).
- It is not known whether or not l-methylfolate can obscure pernicious anemia above 0.1 mg doses, so caution is advised also with this form of folate.
Indications and Usage for VP-ZEL tablets
VP-ZEL Tabs is indicated for the distinct nutritional requirements of patients in need of dietary supplementation as determined by a licensed medical practitioner. VP-ZEL Tabs should be administered under the supervision of a licensed medical practitioner.
This product is contraindicated in patients with a known hypersensitivity to any of the ingredients.
Caution is recommended in patients with a history of bipolar illness.
Folate, when administered as a single agent in doses about 0.1 mg daily, may obscure the detection of vitamin B12 deficiency (specifically, the administration of folic acid may reverse the hematological manifestations of B12 deficiency, including pernicious anemia, while not addressing the neurological manifestations).
Folate therapy alone is inadequate for treatment of a vitamin B12 deficiency.
VP-ZEL Tabs is a prescription dietary supplement to be used only under licensed medical supervision.
Drugs which may interact with folate include:
- Antiepileptic drugs (AED): The AED class including, but not limited to, phenytoin, carbamazepine, primidone, valproic acid, fosphenytoin, valproate, phenobarbital and lamotrigine have been shown to impair folate absorption and increase the metabolism of circulating folate.
- Additionally, concurrent use of folic acid has been associated with enhanced phenytoin metabolism, lowering the level of the AED in the blood and allowing breakthrough seizures to occur. Caution should be used when prescribing this product among patients who are receiving treatment with phenytoin and other anticonvulsants.
- Capecitabine: Folinic acid (5-formyltetrahydrofolate) may increase the toxicity of Capecitabine.
- Cholestyramine: Reduces folic acid absorption and reduces serum folate levels.
- Colestipol: Reduces folic acid absorption and reduces serum folate levels.
- Cycloserine: Reduces folic acid absorption and reduces serum folate levels.
- Dihydrofolate Reductase Inhibitors (DHFRI): DHFRIs block the conversion of folic acid to its active forms, and lower plasma and red blood cell folate levels. DHFRIs include aminopterin, methotrexate, pyrimethamine, triamterene, and trimethoprim.
- Fluoxetine: Fluoxetine exerts a noncompetitive inhibition of the 5-methyltetrahydrofolate active transport in the intestine.
- Isotretinoin: Reduced folate levels have occurred in some patients taking isotretinoin.
- L-dopa, triamterene, colchicine, and trimethoprim may decrease plasma folate levels.
- Nonsteroidal Anti-inflammatory Drugs (NSAIDs): NSAIDs have been shown to inhibit some folate dependent enzymes in laboratory experiments.
- NSAIDs include ibuprofen, naproxen, indomethacin and sulindac.
- Oral Contraceptives: Serum folate levels may be depressed by oral contraceptive therapy.
- Methylprednisolone: Reduced serum folate levels have been noted after treatment with methylprednisolone.
- Pancreatic Enzymes: Reduced folate levels have occurred in some patients taking pancreatic extracts, such as pancreatin and pancrelipase.
- Pentamidine: Reduced folate levels have been seen with prolonged intravenous pentamidine.
- Pyrimethamine: High levels of folic acid may result in decreased serum levels of pyrimethamine.
- Smoking and Alcohol: Reduced serum folate levels have been noted.
- Sulfasalazine: Inhibits the absorption and metabolism of folic acid.
- Metformin treatment in patients with type 2 diabetes decreases serum folate.
- Warfarin can produce significant impairment in folate status after a 6-month therapy.
Drugs which may interact with nicotinamide:
- The clearance of primidone and carbamazepine may be reduced with the concomitant use of nicotinamide.
Drugs which may interact with zinc oxide:
- The absorption of quinolones or tetracycline may be decreased with the concomitant use of zinc.
Drugs which may interact with cupric oxide:
- Concomitant use of penicillamine and copper can cause decreased absorption of both substances.
PREGNANCY and NURSING MOTHERS
VP-ZEL Tabs is not intended for use as a prenatal/ postnatal multivitamin for lactating and nonlactating mothers. Talk with your medical practitioner before using if pregnant or lactating.
Allergic sensitization has been reported following both oral and parental administration of folic acid, and may possibly occur with other forms of folate.
VP-ZEL tablets Dosage and Administration
Usual adult dose is one or two tablets taken once or twice a day with or without food or as directed by a licensed medical practitioner.
How is VP-ZEL tablets Supplied
VP-ZEL Tabs tablets are coated, purple colored, oval-shaped tablets debossed on one side with "V221", and are supplied in bottles of 60 tablets.
Store at Controlled Room Temperature 15°-30° C (59°-86°F).
[See USP]. Protect from light and moisture. Dispense in a tight, light-resistant container.
KEEP THIS OUT OF REACH OF CHILDREN.
All prescriptions using this product shall be pursuant to state statutes as applicable. This is not an Orange Book product.
Call your licensed medical practitioner about side effects.
You may report side effects by calling 813-283-1344.
Prescription Dietary Supplement
Tampa, FL 33619
MADE IN USA
- These products are dietary supplements that - due to increased folate levels (AUG 3 1973 FR 20750), require an Rx on the label because of increased risk associated with masking of B12 deficiency. As such this product requires licensed medical supervision, an Rx status, and a national drug code (NDC) as required by pedigree reporting requirements.
PRINCIPAL DISPLAY PANEL - 60 Tablet Bottle Label
Prescription Dietary Supplement
Made in the USA
niacinamide, azelaic acid, zinc, pyridoxine, cupric oxide, and folic acid tablet, coated
|Labeler - Virtus Pharmaceuticals (969483143)|