Boostervite

Boostervite is an FDA-registered drug product whose active ingredient is MULTIVITAMIN. It is labelled by PureTek Corporation taken by oral and marketed as a human prescription drug product. Identifiers on file: NDC 59088-022, label effective 20260618. It is one of 6 FDA drug label records sharing the active ingredient MULTIVITAMIN. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

Across FDA labelling, products containing MULTIVITAMIN are most often described in connection with: usage boostervite, contains combination, vitamins minerals, botanical extracts, intended supplement, nutritional intake, low energy, supervision healthcare. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

INDICATIONS AND USAGE: 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.

WARNING: 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.

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.

FDA lists 6 drug label records with MULTIVITAMIN as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

What is Boostervite used for?
INDICATIONS AND USAGE: 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.

Who makes Boostervite?
PureTek Corporation is the labeler of record for Boostervite. 6 FDA label records share the active ingredient MULTIVITAMIN, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does Boostervite come in?
administered by oral. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is Boostervite prescription or over-the-counter?
The FDA label for this product is recorded as human prescription drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Are there other products containing MULTIVITAMIN?
Yes. 6 FDA drug label records list MULTIVITAMIN as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has Boostervite been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.