HEMAX

Manufacturer
Pronova Corporation
Effective date
2024-08-07
Label type
DIETARY SUPPLEMENT
Version
1
Source
full-release
Hydrated at
2026-06-01 02:51:07

Label at a glance#

ProductHEMAX
Active ingredientASCORBIC ACID, .ALPHA.-TOCOPHEROL ACETATE, DL-, LEVOMEFOLATE CALCIUM, CYANOCOBALAMIN, BIOTIN, IRON, CUPRIC SULFATE
Label structure7 sections

Dosage and administration

One tablet 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: 90
Amount% Daily
Per ServingValue 
 Vitamin C (as Ascorbic Acid)500 mg 556% 
 Vitamin E (as dl-Alpha Tocopheryl Acetate)13.5 mg 90% 
 Folate (as L-5-methyltetrahydrofolate Calcium)1,020 mcg DFE 255% 
(600 mcg L-5-MTH) 
 Vitamin B12 (as Cyanocobalamin)60 mcg 2,500%
 Biotin150 mcg 500% 
 Iron (as Carbonyl Iron)150 mg 833% 
 Copper (as Cupric Sulfate)3 mg 333% 
 *Daily Value not established

OTHER INGREDIENTS: Microcrystalline Cellulose, Citric Acid, Stearic Acid, Dicalcium Phosphate, Croscarmellose Sodium, Polyvinylpyrrolidone, Hypromellose, Magnesium Stearate, Silicon Dioxide, Starch, Glucose, Calcium Carbonate, Crospovidone, Isomalt, Sodium Lauryl Sulfate, Maltodextrin, Triglycerides, Sucrose, Soy Polysaccharide, Glycerin, Mineral Oil, Polyethylene Glycol, Artificial French Vanilla Flavor, Annatto Extract (color), Propylene Glycol, Tricalcium Phosphate, Potassium Hydroxide and Talc. Contains soy, a bioengineered food ingredient.

HEMAXTM 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 a leading cause of fatal poisoning in children under 6 years of age. KEEP THIS PRODUCT OUT OF THE REACH OF CHILDREN. In case of accidental overdose, call a doctor or poison control center immediately.

DO NOT USE HEMAXTM for individuals with a known hypersensitivity to any of the ingredients. Hemochromatosis and hemosiderosis are contraindications to iron therapy. This product is not for use in children under 12 years of age.

WARNING:

Consuming this product can expose you to chemicals including, lead and mercury, which are known to the State of California to cause cancer and birth defects or other reproductive harm. For more information go to www.P65Warnings.ca.gov/food.

CAUTION:

PRECAUTIONS SECTION

This product contains 1.7mg DFE (1mg) of 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 B12 is deficient. Folic acid in amounts above 0.1 mg daily may obscure pernicious anemia in that hematologic remission can occur while neurological manifestations remain progressive. Allergic sensitization has been reported following both oral and parenteral administration of folic acid. Pregnant women, nursing mothers or women prior to conception who take HEMAXTM 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 tablet daily with or without food or as recommended by your healthcare provider.

OTHER INFORMATION:

SAFE HANDLING WARNING SECTION

HEMAXTM is supplied in child-resistant bottles of 90, 30 and 4 tablets. Store at room temperature, USP.

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

Manufactured in the USA for:

Pronova Corporation
Miami, Florida 33155

HEALTH CLAIM SECTION

DIETARY SUPPLEMENT

With 100% Bioactive Folate

EZY-DOSE TABLETS

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

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HEMAXHEMAX

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
b82b4008-22fd-05f5-6cc6-c0a6e81c65b8Product name220240805
910c1bd7-67d1-44c7-ad4f-9445f827edccProduct name120230808
cb89b86a-369e-4204-8910-ae797c503af3Product name120230706
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
d4880ace-a516-8c47-8dfd-73a4ba5887d7Product name220180830
ddff2484-d547-4e6a-bacd-95eef7e31c64Product name220180807
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
90854981-3820-4bc4-a1d3-666ec508941cProduct name220180214
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122
d206bb34-ea65-399d-70d9-834f22dc2c18Product name320170724
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
67555-131-30HEMAX30 in 1 BOTTLETABLET301
67555-131-90HEMAX90 in 1 BOTTLETABLET901

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
67555-131HEMAX (ASCORBIC ACID, DL-ALPHA TOCOPHERYL ACETATE, L-5-METHYLTETRAHYDROFOLATE CALCIUM, CYANOCOBALAMIN, BIOTIN, CARBONYL IRON, CUPRIC SULFATE) TABLET [PRONOVA CORPORATION]12 package rows20240820_60a9b750-daf3-4f4c-a0fa-93e73edcc744.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
67555-131-90EA - Each67555-1316c52fdb7-e22c-4da4-82c7-b9f1222ef8a612024-11-05

Products#

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

DailyMed product names page 1 of 1 · 39 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
67555-13167555-131-30, 67555-131-90

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 34 matching rows.

Source Document#

Source XML

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 · 4 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Ascorbic AcidASCORBIC ACIDRenova Pharmaceuticals LLCa6481bae-2397-44c7-a51d-4f47ad91bd2c2026-08-19Warnings, Adverse reactionsName fallback
generic name: ASCORBIC ACID
AscorASCORBIC ACIDMcGuff Pharmaceuticals, Inc.388aad52-fc01-4784-9791-1dbc80c693062026-05-29Warnings, Adverse reactionsName fallback
generic name: ASCORBIC ACID
Ascorbic AcidASCORBIC ACIDFresenius Kabi USA, LLC1606e29f-0e80-4069-b688-daab9cbff20a2025-12-17Warnings, Adverse reactionsName fallback
generic name: ASCORBIC ACID
Skin Renewing SerumASCORBIC ACIDGuangzhou Danting Bath&Body Care Industry Co. Ltd396c2a8d-ac95-cbef-e063-6294a90aff392025-08-23WarningsName fallback
generic name: ASCORBIC ACID

Reported adverse events (FAERS/openFDA)#

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