MaxFe

Manufacturer
Pronova Corporation
Effective date
2023-05-16
Label type
DIETARY SUPPLEMENT
Version
2
Source
full-release
Hydrated at
2026-06-01 02:50:45

Label at a glance#

ProductMaxFe
Active ingredientMAGNESIUM ASCORBATE, LEVOMEFOLATE CALCIUM, CYANOCOBALAMIN, BIOTIN, FERROUS BISGLYCINATE, ZINC GLYCINATE
Label structure7 sections

Dosage and administration

One caplet daily with or without food or as recommended by your healthcare provider.

Label contents#

Full prescribing information#

STATEMENT OF IDENTITY SECTION

 Supplement Facts
 Serving Size: 1 Tablet / Servings Per Container: 120
Amount

Per Serving

% Daily

Value

 Vitamin C (as Magnesium Ascorbate) 100 mg 111%
 Folate (as L-5 Methyltetrahydrofolate
 Calcium)
 1.7 mg DFE 425%
 Vitamin B12 (as Cyanocobalamin) 60 mcg 2500%
 Biotin 150 mcg 500%
 Iron (as Carbonyl Iron and Ferrous Bisglycinate
 Chelate (Ferrochel®))
 160 mg 889%
 Zinc (as Zinc bis-glycinate chelate -TRAACS®)# 12 mg 109%
 * Daily Value not established

OTHER INGREDIENTS: Microcrystalline Cellulose, Dicalcium Phosphate, Citric Acid, Stearic Acid, Croscarmellose Sodium, Silicon Dioxide, Magnesium Stearate, Pharmaceutical Glaze, Crospovidone, Sodium Benzoate, Sodium Lauryl Sulfate, Soy Polysaccharide, Polyvinylpyrrolidone, Maltodextrin, Sucrose, Hypromellose, Polyethylene Glycol, FD&C Yellow #6 Lake, Artificial French Vanilla Flavor, Propylene Glycol, Starch, Tricalcium Phosphate and Talc.

Contains: Soy

DESCRIPTION: MaxFeTM is a multivitamin / multimineral dietary supplement indicated for use in improving the nutritional status of patients with iron deficiency.†

†This statement has not been evaluated by the FDA. This product is not intended to diagnose, treat, cure, or prevent any disease.

WARNINGS SECTION

WARNING: Accidental overdose of iron-containing products is leading a cause of fatal poisoning in children under 6 years of age. KEEP THIS PRODUCT OUT OF REACH OF CHILDREN. In case of accidental overdose, call a doctor or poison control center immediately.

DO NOT USE MAXFeTM for individuals with a known hypersensitivity to any of the ingredients. Patients with hemochromatosis and hemosiderosis. The product is not for use in children under 12 years of age.

CAUTION:

PRECAUTIONS SECTION

This product contains 1 mg folic acid, the maximum safe Reference Daily Intake (RDI) amount for this nutrient. Folic Acid alone should not be used for individuals with pernicious anemia and other megaloblastic anemias where Vitamin B-12 is deficient. Folic acid in amounts above 0.1 mg daily may obscure pernicious anemia in that hematologic remission can occur while neurological manifestations progress. Pregnant women, nursing mothers or women prior to conception who take MAXFeTM should take this supplement only after their medical condition and other drugs, herbs and/or supplements consumption are considered. Use for elderly individuals should be cautious due to the greater frequency of decreased hepatic, renal, or cardiac function.

ADVERSE REACTIONS: Allergic sensitization has been reported following both oral and parenteral administration of folic acid.

DIRECTIONS FOR USE:

DOSAGE & ADMINISTRATION SECTION

One caplet daily with or without food or as recommended by your healthcare provider.

OTHER INFORMATION:

SAFE HANDLING WARNING SECTION

MAXFeTM is supplied in child-resistant trade bottles of 120 and 30 caplets and physician samples in child-resistant bottles of 4 caplets. Store at controlled room temperature 59°-86°F. See USP Controlled Room Temperature.

To report a serious advent event or to obtain product information, contact (866) 703-3508.

Distributed by:

Pronova Corporation
Miami, Florida 33155

HEALTH CLAIM SECTION

Fe With FERROCHEL®

Vitamin & Mineral Supplement with Iron

Bilayered Hematinic Caplets

DO NOT USE IF IMPRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING.

EP2008/052034
#Ferrochel® TRAACS® are registered
trademark of Albion Laboratories, Inc.,
covered by U.S.
Patents 6,716,814
and 7,838,042.

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MaxFe-141MaxFe-141

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
ASCORBIC ACID Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813
CYANOCOBALAMIN Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813
LEVOMEFOLIC ACID Pharmacologic Class Indexing1Indexing - Pharmacologic Class20230428
ZINC CATION Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f47a510b-6679-4664-b2d6-47b5c4afe7ccProduct name420260217
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
b82b4008-22fd-05f5-6cc6-c0a6e81c65b8Product name220240805
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
ddff2484-d547-4e6a-bacd-95eef7e31c64Product name220180807
90854981-3820-4bc4-a1d3-666ec508941cProduct name220180214
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122
d206bb34-ea65-399d-70d9-834f22dc2c18Product name320170724
190f2a5b-bbc8-65c7-fcb0-97891307b917Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
67555-141-12MaxFe120 in 1 BOTTLETABLET1202

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
67555-141MAXFE (MAGNESIUM ASCORBATE, L-5 METHYLTETRAHYDROFOLATE CALCIUM, CYANOCOBALAMIN, BIOTIN, CARBONYL IRON, FERROUS BISGLYCINATE CHELATE, ZINC BIS-GLYCINATE CHELATE) TABLET [PRONOVA CORPORATION]21 package rows20230519_ac33b517-e576-43f1-8097-6af59c508584.zip

Products#

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

DailyMed product names page 1 of 1 · 34 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
67555-14167555-141-12

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 28 matching rows.

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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