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Boostervite
multivitamin · Boostervite is a vitamin c (prescription) containing multivitamin, made by PureTek Corporation.
- Type
- Prescription
- Drug class
- Vitamin C
- Route
- Oral
- Manufacturers
- 1
Boostervite™ contains a combination of vitamins, minerals, and botanical extracts intended to supplement nutritional intake in patients with low energy associated with nutritional needs, under the supervision of a healthcare provider.
Related recalls
FDA drug recalls that name this drug or its active ingredient
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- Class IDrugOngoing09/09/2026Glutathione 200 mg/mL, 30 mL sterile multidose vial, Each vial contains: Glutathione, Ascorbic Acid...OPTIMAL BALANCE PHARMACY · Microbial Contamination of Sterile Products - out of...
- Class IDrugOngoing08/19/2026Glutathione (MDV), 200 mg/mL, 30 mL vial, each mL contains Glutathione 200 mg, Ascorbic Acid 20 mg, Benzyl...Victory Medical Center Pharmacy · Microbial Contamination of Sterile Products - out of...
- Class IIDrugOngoing10/15/2025Ascorbic Acid (Vitamin C) for Injection, Preservative Free, all strengths and presentations, GenoGenix...GenoGenix LLC · 3 products · Lack of Assurance of Sterility
- Class IDrug11/13/2024Ascorbic Acid Inj. Solution, 25,000mg/50mL (500mg/mL), 50mL single use vial, Rx only, Staska...Staska Pharmaceuticals, Inc. · Presence of Particulate Matter: Presence of glass particulates.
Uses
Boostervite™ contains a combination of vitamins, minerals, and botanical extracts intended to supplement nutritional intake in patients with low energy associated with nutritional needs, under the supervision of a healthcare provider.
Dosage and administration
Take one (1) tablet daily with food, or as directed by a healthcare provider. Dosage may be adjusted based on individual patient requirements and clinical response. Do not exceed the recommended dose.
Contraindications
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.
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 folate alone is improper therapy for pernicious anemia and other megaloblastic anemias in which vitamin B12 is deficient.
Precautions
Folate 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 folate to patients with undiagnosed anemia, since folate may obscure the diagnosis of pernicious anemia by alleviating the hematologic manifestations of the disease while allowing the neurological complications to progress. This may result in severe nervous system damage before the correct diagnosis is made. Adequate doses of vitamin B12 may prevent, halt, or improve the neurological changes caused by pernicious anemia. The patient’s medical conditions and consumption of other drugs, herbs, and/or supplements should be considered. Use with caution in patients receiving sedatives, antihypertensive agents, antidiabetic medications, thyroid hormone therapy, or immunosuppressive therapy, as ashwagandha may potentiate pharmacologic effects. To be used only under the supervision of a healthcare provider. Drug Interactions: Boostervite™ is not recommended for use in patients receiving levodopa, as pyridoxine may antagonize the effects of levodopa. Pyridoxine may antagonize levodopa effects. It may also increase bleeding risk with anticoagulants (e.g., heparin, warfarin) or antiplatelet agents (e.g., aspirin, clopidogrel). Adverse Reactions: Allergic sensitization and other hypersensitivity reactions have been reported with oral folate supplementation. Ferrous Fumarate: Gastrointestinal disturbances, including anorexia, nausea, diarrhea, and constipation, have been reported. These effects are generally mild and may resolve with continued use. Administration of Boostervite™ with food may reduce the occurrence of gastrointestinal disturbances, although iron absorption may be decreased when taken with meals. 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. Call your healthcare provider for medical advice about side effects. You may report side effects to PureTek Corporation at 1-877-921-7873. You may also report side effects to FDA at 1-800-FDA-1088 or at www.fda.gov/medwatch.
Side effects (adverse reactions)
Allergic sensitization and other hypersensitivity reactions have been reported with oral folate supplementation. Ferrous Fumarate: Gastrointestinal disturbances, including anorexia, nausea, diarrhea, and constipation, have been reported. These effects are generally mild and may resolve with continued use. Administration of Boostervite™ with food may reduce the occurrence of gastrointestinal disturbances, although iron absorption may be decreased when taken with meals. 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. Call your healthcare provider for medical advice about side effects. You may report side effects to PureTek Corporation at 1-877-921-7873. You may also report side effects to FDA at 1-800-FDA-1088 or at www.fda.gov/medwatch.
Drug interactions
Boostervite™ is not recommended for use in patients receiving levodopa, as pyridoxine may antagonize the effects of levodopa. Pyridoxine may antagonize levodopa effects. It may also increase bleeding risk with anticoagulants (e.g., heparin, warfarin) or antiplatelet agents (e.g., aspirin, clopidogrel).
Use in specific populations
The formula’s safety and efficacy have not been established in certain populations. Safety and effectiveness in pregnant or nursing women, pediatric patients, and geriatric patients have not been established. Use in these populations should be under the supervision of a healthcare provider.
Overdose
OVERDOSE: Signs and symptoms: Iron is toxic in excessive amounts. Acute ingestion of iron may cause nausea, vomiting, abdominal pain, and in severe cases, gastrointestinal bleeding, shock, cardiovascular collapse, and death. Other symptoms may include pallor, cyanosis, melena (black tarry stools), drowsiness, and coma. Severe reactions, including fatalities, have occurred in children from accidental overdose. The estimated toxic dose of orally ingested elemental iron is approximately 300 mg/kg body weight. Treatment: For management of iron overdosage, initiate appropriate supportive and symptomatic therapy. Gastric lavage may be performed using sodium bicarbonate solution or milk. Intravenous fluids and electrolyte replacement should be administered as indicated. Oxygen therapy may be required. In cases of severe toxicity, chelation therapy with appropriate agents (e.g., deferoxamine) should be considered. Exchange transfusion may be indicated in life-threatening situations. Management should be guided by a healthcare provider based on clinical status and laboratory parameters.
Description
Each Tablet Contains: Vitamin C (as ascorbic acid)……………….……………… 100 mg Vitamin D3 (as cholecalciferol)…………….……. 10 mcg (400 IU) Thiamin (as thiamine mononitrate)…………...……………. 10 mg Riboflavin ...................…………………………...………….. 10 mg Niacin (as niacinamide)…………………………....…………10 mg Vitamin B6 (as pyridoxine hydrochloride)………….……….10 mg Folate (as L-5-Methyltetrahydrofolate calcium salt)……….. 1700 mcg DFE (1000 mcg L-5-Methylfolate) Vitamin B12 (as methylcobalamin)………………….….... 100 mcg Biotin (as d-Biotin)……………………...…….................... 300 mcg Pantothenic Acid (as d-Calcium Pantothenate)………....… 50 mg Iron (as Ferrous Fumarate)……………………………......... 18 mg Withania somnifera (Ashwagandha) Root Powder….....…. 60 mg Brassica oleracea acephala (Kale) Powder……….…...…. 2.5 mg Brassica oleracea italica (Broccoli) Sprout Powder..…...... 2.5 mg Citrus sinensis (Orange) Juice Powder……....................... 2.5 mg Prunus cerasus (Tart Cherry) Extract................................. 2.5 mg Other Ingredients: Croscarmellose Sodium, Dicalcium Phosphate, Magnesium Stearate (vegetable source), Microcrystalline Cellulose, Silicon Dioxide, Stearic Acid (vegetable source), Coating (Hydroxypropyl Methylcellulose, Polyethylene Glycol 400, Organic Maltodextrin, Organic Sunflower Lecithin, Organic Sunflower Oil, Organic Guar Gum).
How supplied
Boostervite™ tablets are yellow to brown, speckled, film-coated tablets, supplied in bottles of 30 tablets (NDC 59088-022-54). Dispense in a tight, light-resistant container as defined in the USP/NF, with a child-resistant closure. Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature]. Protect from light and moisture.
Storage and handling
Do not use if the seal under the bottle cap is broken. KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN.
Forms and strengths
From the FDA NDC Directory · 1 product codes
| Dosage form | Strength | Route | NDCs |
|---|---|---|---|
| Tablet | 18 mg / 50 mg / 2.5 mg / 300 ug / 10 mg / 10 mg / 100 mg / 1000 ug / 100 ug / 10 mg / 10 mg / 10 ug / 2.5 mg / 2.5 mg / 2.5 mg / 60 mg | oral | 1 |
Side effect reports to FDA
FDA Adverse Event Reporting System (FAERS), 49,767 reports that list multivitamin, data through 07/30/2026
Anyone can report a problem to FDA, and a report does not mean the drug caused the problem. Reports can be duplicated or incomplete, and counts depend on how widely a drug is used. Do not stop or change a medicine because of this list. Talk to your doctor or pharmacist.
Most often reported reactions
- Fatigue3,691
- Nausea3,248
- Drug ineffective3,160
- Diarrhea2,822
- Headache2,608
- Dizziness2,308
- Dyspnea2,048
- Pain1,937
- Asthenia1,850
- Fall1,750
To report a side effect, use FDA MedWatch.
Manufacturers and labels
1 FDA label
- PureTek CorporationShown hereLabel 06/18/2026 · NDC 59088-022Full label
Boostervite: common questions
- What is Boostervite used for?
- Boostervite™ contains a combination of vitamins, minerals, and botanical extracts intended to supplement nutritional intake in patients with low energy associated with nutritional needs, under the supervision of a healthcare provider.
- What are the side effects of Boostervite?
- Allergic sensitization and other hypersensitivity reactions have been reported with oral folate supplementation. See the full side effects section on this page, and ask your doctor or pharmacist about any side effect that bothers you.
- Is Boostervite a prescription drug?
- Yes. Boostervite is a prescription (Rx) drug.
- Who makes Boostervite?
- PureTek Corporation lists Boostervite with the FDA.
Source: U.S. Food and Drug Administration, openFDA drug label (SPL) and NDC Directory · Last updated 06/18/2026 · Label text is shown as published by the manufacturer. Not medical advice