Folcyteine

Folcyteine 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 59088-795, label effective 20260708. 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: folic acid, usage folcyteine, indicated vitamin, mineral supplementation, adult men, treat megaloblastic, anemia caused, deficiency including. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Indications and Usage : Folcyteine™ is indicated as a vitamin, mineral supplementation for adult men and women. Folic acid is used to treat megaloblastic anemia caused by folic acid deficiency, including cases associated with tropical or nontropical sprue, as well as anemia due to nutritional deficiency or pregnancy.

Dosage and Administration : One (1) Folcyteine™ caplet daily or as directed by a physician. Do not administer to children under the age of 12.

Contraindications : This product is contraindicated in patients with a known hypersensitivity to any of the ingredients. Folcyteine™ is contraindicated in patients with hypercalcemia, malabsorption syndrome, abnormal sensitivity to the toxic effects of vitamin D, and hypervitaminosis D.

Warnings : Patients with kidney disease or thyroid disease should consult a physician or healthcare provider before using this product. Use during pregnancy or breast-feeding only as directed. Administration of folic acid alone is improper therapy for pernicious anemia and other megaloblastic anemias caused by vitamin B12 deficiency.

Adverse Reactions : Allergic sensitization has been reported following both oral and parenteral administration of folic acid. To report side effects, call PureTek Corporation at 1-877-921-7873 or FDA at 1-800-FDA-1088 or 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 Folcyteine used for?
Indications and Usage : Folcyteine™ is indicated as a vitamin, mineral supplementation for adult men and women. Folic acid is used to treat megaloblastic anemia caused by folic acid deficiency, including cases associated with tropical or nontropical sprue, as well as anemia due to nutritional deficiency or pregnancy.

Who makes Folcyteine?
PureTek Corporation is the labeler of record for Folcyteine. 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 Folcyteine 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 Folcyteine 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 Folcyteine 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.