Mediclarum
Medicine guide

Vitranol Fe

35 ug + 1000 ug + 1500 ug + 3.4 mg + 20 mg + 20 mg + 8 ug + 200 mg + 120 mg + 3… · Tablet

  • Prescription only
  • Blood Coagulation Factor
Made by
PureTek Corporation

Quoted from the official source. Not yet reviewed by Mediclarum — the leaflet in your pack is authoritative.

At a glance

Quoted from the official label · 2023-01-11

What it is

Blood Coagulation Factor

Used for
  • Vitranol FE is indicated for the treatment of iron deficiency anemia and folate deficiency as in extended convalescence, menorrhagia, pregnancy, puberty, excessive blood loss, and advanced age.
Do not take it if

This product is contraindicated in patients with known hypersensitivity to any of its ingredients; also, all iron compounds are contraindicated in patients with hemosiderosis, hemochromatosis, or hemolytic anemias.

All warnings ↓
Good to know
  • Prescription only
  • FDA enforcement reports list no ongoing recall, and none from the last two years, for this product code · checked 2026-10-02
12other products contain Ferrous Fumarate, Folic Acid — compare makers, forms and strengths

Every line above is selected, not written, from the official label. Nothing is reworded. DailyMed

What it is for

  • Vitranol FE is indicated for the treatment of iron deficiency anemia and folate deficiency as in extended convalescence, menorrhagia, pregnancy, puberty, excessive blood loss, and advanced age.
  • Also for treatment of condition in which iron deficiency and vitamin C deficiency occur together, along with a deficient intake or increased need for B-Complex vitamins in chronic and acute illness, as well as cases of metabolic stress, and in convalescence.

From the official label · 2023-01-11 · DailyMed

Do not take it if

  • This product is contraindicated in patients with known hypersensitivity to any of its ingredients; also, all iron compounds are contraindicated in patients with hemosiderosis, hemochromatosis, or hemolytic anemias.
  • Pernicious anemia is a contraindication, as folic acid may obscure its signs and symptoms.

Quoted from the official label, section “Contraindications”.

How to take it

These directions are for this exact strength and form. Another one is different.

  • Adults (persons over 12 years of age) One (1) Vitranol Fe Multivitamin caplet daily, between meals or as directed by a physician. Do not administer to
  • children under the age of 12.

Quoted from the official label, section “Dosage & Administration”.

Other warnings

  • Accidental overdose of iron-containing products is a leading cause of fatal poisoning in
  • children under 6.
  • Keep this product out of reach of children.
  • In case of accidental overdose, call a doctor or poison control center immediately.
  • Administration of folic acid alone is improper therapy for pernicious anemia and other megaloblastic anemias in which vitamin B 12 is deficient.
  • Precaution Section Folic acid in doses above 0.1 mg daily may obscure pernicious anemia, in that hematologic remission can occur while neurological manifestations remain progressive.
  • There is a potential danger in administering folic acid to patients with undiagnosed anemia, since folic acid may obscure the diagnosis of pernicious anemia by alleviating the hematologic manifestations of the disease while allowing the neurologic complications to progress.
  • This may result in severe nervous system damage before the correct diagnosis is made.
  • Adequate doses of vitamin B 12 may prevent, halt, or improve the neurologic changes caused by pernicious anemia.
  • The patient’s medical conditions and consumption of other drugs, herbs, and/or supplements should be considered.
  • For use on the order of a healthcare practitioner.
  • Call your doctor about side effects.
  • To report side effects, call PureTek Corporation at 1-877-921-7873 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.
  • Drug Interactions:
  • Adverse Reactions:
  • Folic Acid:
  • Precaution Section Folic acid in doses above 0.1 mg daily may obscure pernicious anemia, in that hematologic remission can occur while neurological manifestations remain progressive.
  • There is a potential danger in administering folic acid to patients with undiagnosed anemia, since folic acid may obscure the diagnosis of pernicious anemia by alleviating the hematologic manifestations of the disease while allowing the neurologic complications to progress.
  • This may result in severe nervous system damage before the correct diagnosis is made.
  • Adequate doses of vitamin B 12 may prevent, halt, or improve the neurologic changes caused by pernicious anemia.
  • The patient’s medical conditions and consumption of other drugs, herbs, and/or supplements should be considered.
  • For use on the order of a healthcare practitioner.
  • Call your doctor about side effects.
  • To report side effects, call PureTek Corporation at 1-877-921-7873 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

Quoted from the official label, section “Warnings”.

Other medicines

  • Vitranol FE is not recommended for and should not be given to patients receiving levodopa because the action of levodopa is antagonized by pyridoxine.
  • There is a possibility of increased bleeding due to pyridoxine interaction with anticoagulants (e.g., Aspirin, Heparin, or Clopidogrel).

Quoted from the official label, section “Drug Interactions”.

If you take too much

In an emergency, call your local emergency number or a poison control centre.

  • OVERDOSE: Iron: Signs and Symptoms: Iron is toxic.
  • Acute overdosage of iron may cause nausea and vomiting and, in severe cases, cardiovascular collapse and death.
  • Other symptoms include pallor and cyanosis, melena, shock, drowsiness, and coma.
  • The estimated overdose of orally ingested iron is 300 mg/kg body weight.
  • When overdoses are ingested by children, severe reactions, including fatalities, have resulted.
  • Vitranol FE should be stored beyond the reach of children to prevent against accidental iron poisoning.
  • Keep this and all other drugs out of reach of children.
  • Treatment:
  • For specific therapy, exchange transfusion and chelating agents should be used.
  • For general management, perform gastric lavage with sodium bicarbonate solution or milk.
  • Administer intravenous fluids and electrolytes and use oxygen.

Quoted from the official label, section “Overdosage”.

Side effects

  • Folic Acid:
  • Allergic sensitizations have been reported following both oral and parenteral administration of folic acid.
  • Ferrous Fumarate:
  • Gastrointestinal disturbances (anorexia, nausea, diarrhea, constipation) occur occasionally, but are usually mild and may subside with continuation of therapy.
  • Although the absorption of iron is best when taken between meals, giving Vitranol FE after meals may control occasional gastrointestinal disturbances.
  • Vitranol FE is best absorbed when taken at bedtime.
  • Adverse reactions have been reported with specific vitamins and minerals but generally at levels substantially higher than those contained herein.
  • However, allergic and idiosyncratic reactions are possible at lower levels.
  • Iron, even at the usual recommended levels, has been associated with gastrointestinal intolerance in some patients.

Quoted from the official label, section “Adverse Reactions”.

What it looks like and how it is packed

  • Vitranol FE are beige speckled, oblong, coated caplets, in bottles containing 30 caplets – NDC 59088-173-54.
  • Dispense in a tight, light-resistant container as defined in the USP/NF with a child-resistant closure.
  • Store at controlled room temperature 20° to 25°C (68° to 77°F). [See USP].
  • Protect from light and moisture and avoid excessive heat.

Quoted from the official label, section “How Supplied”.

How to store it

  • Do not use if bottle seal is broken.
  • KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN.
  • Store at controlled room temperature 20° to 25°C (68° to 77°F). [See USP].
  • Protect from light and moisture and avoid excessive heat.
  • To report a serious adverse event or to obtain product information, contact 877-921-7873.

Quoted from the official label, section “Storage and Handling”.

What is in it

  • Each caplet contains:
  • Vitamin A (as retinyl acetate)……………….. 1500 mcg (5000 IU) Vitamin C (as ascorbic acid)……………………………… 120 mg Vitamin D3 (as cholecalciferol)………………….. 20 mcg (800 IU) Vitamin E (dl-alpha tocopheryl acetate)…………… 30 mg (30 IU) Thiamin (as thiamine mononitrate)…………………………. 3 mg Riboflavin (vitamin B2)……………………………………. 3.4 mg Niacin (as niacinamide)…………………………………… 20 mg Vitamin B6 (as pyridoxine hydrochloride)…………………. 20 mg Folate (as folic acid)……….. 1700 mcg DFE (1000 mcg folic acid) Vitamin B12 (as cyanocobalamin)………………………….. 8 mcg Calcium (as calcium carbonate)…………………………. 200 mg Iron (as ferrous fumarate)………………………………… 27 mg Magnesium (as magnesium oxide)……………………… 200 mg Zinc (as zinc oxide)……………………………………….. 25 mg Selenium (as selenium amino acid chelate)………………. 55 mcg Manganese (as manganese sulfate)……………………… 2.3 mg Chromium (as chromium polynicotinate)……………….. 35 mcg Molybdenum (as molybdenum amino acid chelate)……… 45 mcg Other Ingredients:
  • Organic cocoa powder, croscarmellose sodium, crospovidone, magnesium stearate, microcrystalline cellulose, silicon dioxide, stearic acid.
  • Clear coating: (hydroxypropyl methylcellulose, PEG-8).

Quoted from the official label, section “Description”.

Ingredients people check for

Lactose, gluten, dyes, sugars and other ingredients that matter with an allergy, intolerance or diet — as this product’s FDA label lists them.

The stored label for this product has no list of inactive ingredients. The list on the pack is the one to check.

Quoted from the FDA label. A label that does not name an ingredient is not a guarantee that the product is free of it, and formulations change. With an allergy, check the pack and ask a pharmacist.

Every version of this medicine (5)

The same active substance, strength and kind of form, from every company that sells it — with what each label lists.

Showing 5 of 5

Details

Made byPureTek Corporation
Active substanceFerrous Fumarate, Folic Acid
Used inDigestion, stomach, diabetes and nutrition
Strength35 ug + 1000 ug + 1500 ug + 3.4 mg + 20 mg + 20 mg + 8 ug + 200 mg + 120 mg + 3…
FormTablet
RouteOral
Packs30 TABLET in 1 BOTTLE, PLASTIC
NDC59088-173

Source: NDC Directory · 2026-09-13 · not reviewed by a clinician

Source: US Food and Drug Administration, NDC Directory. Reuse terms: US government work (FDA).

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Same active substance

These contain the same substance. That does not mean one can replace another — ask a pharmacist.

Foliflex1500 ug + 250 mg + 13.75 ug + 45 mg + 3.25 mg + 3.35 mg + 22.5 mg + 6 mg + 500…Prescription onlyTablet PureTek Corporation · Ferrous Fumarate, Folic AcidFolitin-Z1500 ug + 250 mg + 13.75 ug + 45 mg + 3.25 mg + 3.35 mg + 22.5 mg + 6 mg + 500…Prescription onlyTablet PureTek Corporation · Ferrous Fumarate, Folic AcidPrenatrix27 mg + 25 mg + 50 ug + 55 mg + 45 ug + 70 ug + 150 ug + 200 mg + 2.6 mg + 1500…Prescription onlyTablet PureTek Corporation · Ferrous Fumarate, Folic AcidPrenatryl200 mg + 2.6 mg + 1500 ug + 120 mg + 20 ug + 30 mg + 3 mg + 3.4 mg + 20 mg + 50…Prescription onlyTablet PureTek Corporation · Ferrous Fumarate, Folic AcidPretrate200 mg + 2.6 mg + 1500 ug + 120 mg + 20 ug + 30 mg + 3 mg + 3.4 mg + 20 mg + 50…Prescription onlyTablet PureTek Corporation · Ferrous Fumarate, Folic AcidPrometa200 mg + 2.6 mg + 1500 ug + 120 mg + 20 ug + 30 mg + 3 mg + 3.4 mg + 20 mg + 50…Prescription onlyTablet PureTek Corporation · Ferrous Fumarate, Folic Acid

See every product with Ferrous Fumarate, Folic Acid