Vitafol Fe Plus
200 mg + 15 mg + 9 mg + 25 mg + 330 ug + 60 mg + 1.6 mg + 1.8 mg + 2.5 mg + 25… · Capsule, Liquid Filled
- Prescription only
- Calculi Dissolution Agent
- Made by
- Exeltis USA, Inc.
- Source
- Official label
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 · 2025-03-20
Calculi Dissolution Agent
- Vitafol ® Fe + prenatal supplement provides vitamin, mineral and omega-3 fatty acid supplementation throughout pregnancy, including individuals with known allergies to fish.* Vitafol ® Fe + does not contain…
Accidental overdose of iron-containing products is a leading cause of fatal poisoning in
All warnings ↓- Prescription only
- FDA enforcement reports list no ongoing recall, and none from the last two years, for this product code · checked 2026-10-02
Every line above is selected, not written, from the official label. Nothing is reworded. DailyMed
What it is for
USAGE:
- Vitafol ® Fe + prenatal supplement provides vitamin, mineral and omega-3 fatty acid supplementation throughout pregnancy, including individuals with known allergies to fish.* Vitafol ® Fe + does not contain fish oils, fish proteins, or fish by-products.
From the official label · 2025-03-20 · DailyMed
Serious warning
The strongest warning the FDA requires. It is printed in a box at the top of the label.
- 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 a Poison Control Center immediately.
Quoted from the official label, section “Boxed Warning”.
Do not take it if
- Vitafol ® Fe + prenatal supplement is contraindicated in patients with hypersensitivity to any of its components or color additives.
- Folic acid is contraindicated in patients with untreated and uncomplicated pernicious anemia, and in those with anaphylactic sensitivity to folic acid.
- Iron supplementation is contraindicated in patients with hemochromatosis and patients with iron storage disease or the potential for iron storage disease due to chronic hemolytic anemia (e.g., inherited anomalies of hemoglobin structure or synthesis and/or red cell enzyme deficiencies, etc.), pyridoxine responsive anemia, or cirrhosis of the liver.
- Cyanocobalamin is contraindicated in patients with sensitivity to cobalt or to cyanocobalamin (vitamin B12).
Quoted from the official label, section “Contraindications”.
How to take it
These directions are for this exact strength and form. Another one is different.
Take one softgel capsule by mouth daily during pregnancy, or as directed by a physician.
Quoted from the official label, section “Dosage & Administration”.
Other warnings
- /PRECAUTIONS: This product is intended for use as directed by your healthcare provider.
- Do not share with others.
- Vitafol ® Fe + must be used with caution in patients with known sensitivity or allergy to soy.
- Vitamin D supplementation should be used with caution in those with hypercalcemia or conditions that may lead to hypercalcemia such as hyperparathyroidism and those who form calcium-containing kidney stones.
- High doses of vitamin D can lead to elevated levels of calcium that reside in the blood and soft tissues.
- Bone pain, high blood pressure, formation of kidney stones, renal failure, and increased risk of heart disease can occur.
- Iodine should be used with caution in patients with an overactive thyroid.
- Prolonged use of iron salts may produce iron storage disease.
- Folic acid, especially in doses above 0.1 mg daily, may obscure pernicious anemia, in that hematologic remission may occur while neurological manifestations remain progressive.
- The use of folic acid doses above 1 mg daily may precipitate or exacerbate the neurological damage of vitamin B12 deficiency.
- Consumption of more than 3 grams of omega-3 fatty acids per day from all sources may lead to excessive bleeding.
- Supplemental intake of omega-3 fatty acids such as DHA exceeding 2 grams per day is not recommended.
- Avoid Overdosage.
- Keep out of the reach of children.
- DRUG INTERACTIONS Medications for an overactive thyroid (anti-thyroid drugs) used in conjunction with iodine supplementation may lead to hypothyroidism.
- Consult appropriate references for additional specific vitamin-drug interactions INFORMATION FOR PATIENTS Patients should be counseled to disclose all medical conditions, including use of all medications, vitamins and supplements, pregnancy, and breast-feeding.
- PEDIATRIC USE Not for pediatric use.
Quoted from the official label, section “Warnings”.
Other medicines
- Medications for an overactive thyroid (anti-thyroid drugs) used in conjunction with iodine supplementation may lead to hypothyroidism.
- Medications for hypertension used in conjunction with iodine supplementation may increase potassium levels in blood.
- High doses of folic acid may result in decreased serum levels of the anticonvulsant drugs; carbamazepine, fosphenytoin, phenytoin, phenobarbital, valproic acid.
- Folic acid may decrease a patient's response to methotrexate.
- Vitamin D supplementation should not be given with large amounts of calcium in those with hypercalcemia or conditions that may lead to hypercalcemia such as hyperparathyroidism and those who form calcium-containing kidney stones.
- Zinc can inhibit the absorption of certain antibiotics; take at least 2 hours apart to minimize interactions.
- Consult appropriate references for additional specific vitamin-drug interactions
Quoted from the official label, section “Drug Interactions”.
Use in children
Not for pediatric use.
Quoted from the official label, section “Pediatric Use”.
Side effects
- Adverse reactions have been reported with specific vitamins and minerals, but generally at doses substantially higher than those in Vitafol ® Fe + .
- However, allergic and idiosyncratic reactions are possible at any dose.
- Reported adverse events include skin ailments, gastrointestinal complaints, glucose abnormalities, and visual problems.
- You should call your doctor for medical advice about adverse or unexpected reactions.
- To report to the company an adverse event or obtain product information, call 1-877-324-9349.
Quoted from the official label, section “Adverse Reactions”.
What to discuss with your doctor
Patients should be counseled to disclose all medical conditions, including use of all medications, vitamins and supplements, pregnancy, and breast-feeding.
Quoted from the official label, section “Patient Counseling Information”.
What it looks like and how it is packed
- Vitafol ® Fe + is available as a purple, oval shaped softgel capsule imprinted "EX0096".
- Available in box of Unit-Dose pack of 30 (5 child resistant blister cards containing 6 softgel capsules) (0642-7473-30) and as professional samples (0642-7473-01).
- Store at room temperature, approximately 15°-30°C (59°-86°F),
- avoid excessive heat above 30°C (86°F), light and moisture.
Quoted from the official label, section “How Supplied”.
How to store it
- Store at room temperature, approximately 15°-30°C (59°-86°F),
- avoid excessive heat above 30°C (86°F), light and moisture.
Quoted from the official label, section “Storage and Handling”.
What is in it
- COMPOSITION:
- Each Vitafol ® Fe+ softgel capsule contains:
- Vitamin A (as beta carotene) 330 mcg RAE Vitamin C (as ascorbic acid) 60 mg Vitamin D (as cholecalciferol) 25 mcg Vitamin E (as dl-alpha tocopheryl acetate) 9 mg Thiamin (Vitamin B1 as thiamine mononitrate) 1.6 mg Riboflavin (Vitamin B2) 1.8 mg Niacin (as niacinamide) 15 mg NE Vitamin B6 (as pyridoxine hydrochloride) 2.5 mg Folate 1700 mcg DFE (680 mcg DFE from folic acid & 1020 mcg DFE from l-methylfolate calcium) Vitamin B12 (as cyanocobalamin) 25 mg Iron (as polysaccharide iron complex) 90 mg Iodine (as potassium iodide) 150 mcg Magnesium (as magnesium oxide) 20 mg Zinc (as zinc oxide) 25 mg Copper (as copper oxide) 2 mg Docosahexaenoic acid (DHA) (from natural algal oil) 200 mg Other Ingredients:
- Gelatin (Bovine), Soybean Oil, Glycerin, Yellow Beeswax, Sorbitol, Soy Lecithin, Titanium Dioxide (color), FD&C Red #40, FD&C Blue #1 Contains:
- Soy
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.
Details
| Made by | Exeltis USA, Inc. |
|---|---|
| Active substance | Doconexent, Niacinamide, .alpha.-Tocopherol Acetate, Dl-, Cholecalciferol, Beta Carotene, Ascorbic Acid, Thiamine Mononitrate, Riboflavin, Pyridoxine Hydrochloride, Cyanocobalamin, Iron, Zinc Oxide, Cupric Oxide, Potassium Iodide, Magnesium Oxide, Folic Acid, and Levomefolate Calcium |
| Used in | Digestion, stomach, diabetes and nutrition |
| Strength | 200 mg + 15 mg + 9 mg + 25 mg + 330 ug + 60 mg + 1.6 mg + 1.8 mg + 2.5 mg + 25… |
| Form | Capsule, Liquid Filled |
| Route | Oral |
| Packs | 5 BLISTER PACK in 1 BOX, UNIT-DOSE / 6 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
| NDC | 0642-7473 |
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).