Vitramyn Rx

Manufacturer
PureTek Corporation
Effective date
2026-06-18
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
5
Source
monthly-update
Hydrated at
2026-07-17 21:38:55

Label at a glance#

ProductVitramyn
Active ingredientRIBOFLAVIN, NIACINAMIDE, ASCORBIC ACID, FOLIC ACID, CYANOCOBALAMIN, CALCIUM CARBONATE, VITAMIN A ACETATE, THIAMINE MONONITRATE, ZINC OXIDE, MANGANESE SULFATE, .ALPHA.-TOCOPHEROL ACETATE, DL-, MAGNESIUM OXIDE, CHROMIUM NICOTINATE, PYRIDOXINE HYDROCHLORIDE, MOLYBDENUM, SELENIUM, CHOLECALCIFEROL
Label structure9 sections

Indications and uses

Vitramyn™ tablets are formulated to provide daily vitamin supplementation for adult men and women, helping support overall nutritional wellness. With folate, Vitramyn™ may be especially beneficial for women during the pre-pregnancy, pregnancy, and post-pregnancy periods by supporting healthy folate levels and helping address anemia related to folate deficiency.

Dosage and administration

The recommended dosage is one (1) Vitramyn™ tablet daily, taken between meals or as directed by a physician. Vitramyn™ tablets are not recommended for use in children under 12 years of age.

Storage and handling

Do not use if the seal under the bottle cap is broken. KEEP THIS AND ALL MEDICATIONS OUT OF REACH OF CHILDREN.

Label contents#

Full prescribing information#

DESCRIPTION:

DESCRIPTION SECTION

Each tablet contains:

Vitamin A (as retinyl acetate)……………….. 1500 mcg RAE (5000 IU)
Vitamin C (as ascorbic acid)……………….……………… 120 mg
Vitamin D3 (as cholecalciferol)…………….……. 20 mcg (800 IU)
Vitamin E (as dl-Alpha-Tocopheryl Acetate)……….....……. 30 mg
Thiamin (as thiamine mononitrate)…………...……………… 3 mg
Riboflavin.....................…………………………...…………. 3.4 mg
Niacin (as niacinamide)…………………………....………… 20 mg
Vitamin B6 (as pyridoxine hydrochloride)………….………. 20 mg
Folate (as L-5-Methyltetrahydrofolate calcium salt)……….. 1700 mcg DFE (1000 mcg L-5-Methylfolate)
Vitamin B12 (as cyanocobalamin)………………….……….. 8 mcg
Calcium (as calcium carbonate)……………………...……. 200 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:
Croscarmellose sodium, crospovidone, magnesium stearate, microcrystalline cellulose, organic cocoa powder, silicon dioxide, stearic acid, clear coating: hydroxypropyl methylcellulose, polyethylene glycol 400, organic guar gum, organic maltodextrin, organic sunflower lecithin, organic sunflower oil.

INDICATIONS AND USAGE:

INDICATIONS & USAGE SECTION

Vitramyn™ tablets are formulated to provide daily vitamin supplementation for adult men and women, helping support overall nutritional wellness. With folate, Vitramyn™ may be especially beneficial for women during the pre-pregnancy, pregnancy, and post-pregnancy periods by supporting healthy folate levels and helping address anemia related to folate deficiency.

CONTRAINDICATIONS:

CONTRAINDICATIONS SECTION

This product is contraindicated in patients with a known hypersensitivity to any of the ingredients.

WARNING:

WARNINGS SECTION

Administration of folic acid alone is improper therapy for pernicious anemia and other megaloblastic anemias in which vitamin B12 is deficient.

PRECAUTIONS:

PRECAUTIONS SECTION

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 neurologic 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 neurologic changes caused by pernicious anemia.

The patient’s medical conditions and consumption of other drugs, herbs, and/or supplements should be considered.

Drug Interactions:

DRUG INTERACTIONS SECTION

Vitramyn™ 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 antiplatelet
agents (e.g., aspirin, clopidogrel) and anticoagulants (e.g., heparin).

Adverse Reactions:

ADVERSE REACTIONS SECTION

Allergic sensitization has been reported following both oral and parenteral administration of folate derivatives.

Adverse reactions have been reported with individual vitamins and minerals, generally at levels substantially higher than those contained in this product.

However, allergic and idiosyncratic reactions may occur even at lower levels.

Gastrointestinal intolerance (e.g., nausea, abdominal discomfort) has been reported with certain vitamins and minerals, particularly at higher doses.

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.

Dosage and Administration:

DOSAGE & ADMINISTRATION SECTION

The recommended dosage is one (1) Vitramyn™ tablet daily, taken between meals or as directed by a physician.

Vitramyn™ tablets are not recommended for use in children under 12 years of age.

HOW SUPPLIED:

HOW SUPPLIED SECTION

Vitramyn™ is supplied as beige, speckled, oblong, film-coated, caplet-shaped tablets in bottles of 30 (NDC 59088-193-54). Dispense in a tight, light-resistant container as defined in the USP/NF with a child-resistant closure.

Store at controlled room temperature 20°C to 25°C (68°F to 77°F) [see USP Controlled Room Temperature]. Protect from light and moisture. Avoid excessive heat.

STORAGE AND HANDLING SECTION

Do not use if the seal under the bottle cap is broken.

KEEP THIS AND ALL MEDICATIONS OUT OF REACH OF CHILDREN.

Vitramyn™

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Manufactured in the USA by:
PureTek Corporation

Panorama City, CA 91402
Questions? Call toll-free:
1-877-921-7873

labellabel

DailyMed Product Concepts#

Product concept, Relation, Version table
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DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
59088-193-54EA - Each59088-193920d8118-431a-490d-b121-0a8b06ba384b12021-09-07

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 37 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59088-19359088-193-54

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 26 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
42024-12-03full-release2026-05-31 21:18:46

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
VitramynFOLIC ACIDPureTek Corporationc8af7616-5178-6df0-e053-2a95a90a334d2026-06-18Warnings, Adverse reactionsExact identifier
ndc (package): 59088-193-54
ndc (product): 59088-193
ndc11 (package): 59088019354
spl id: 548ee394-41b9-d346-e063-6394a90a0773
spl set id: c8af7616-5178-6df0-e053-2a95a90a334d

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.