HEMATRON-AF- ascorbic acid, dl-alpha tocopheryl acetate, l-5-methyltetrahydrofolate calcium, cyanocobalamin, biotin, carbonyl iron, cupric sulfate tablet

Hematron-AF by

Drug Labeling and Warnings

Hematron-AF by is a Other medication manufactured, distributed, or labeled by Seyer Pharmatec, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

STATEMENT OF IDENTITY

Supplement Facts
Serving Size: 1 Tablet
	Amount	% Daily
	Per Serving	Value
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-MTHF)
Vitamin B12 (as Cyanocobalamin)	60 mcg	2,500%
Biotin	150 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

Contains a bioengineered food ingredient.

HEMATRON AF is a multi-vitamin / multi-mineral 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

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 REACH OF CHILDREN. In case of accidental overdose, call a doctor or poison control center immediately.

DO NOT USE with individuals with a known hypersensitivity to any of the ingredients. Patients with hemochromatosis and hemosiderosis are contra-indications to iron therapy. This product is not for use in children under 12 years of age.

CAUTION:

This product contains 1,020mcg DFE (600mcg L5-MTHF); the maximum safe Reference Daily Intake (RDI) amount for this nutrient is 1000mcg. Folic Acid in doses above 0.1 mg (1000mcg) daily may obscure pernicious anemia in that hematologic remission can occur while neurologic manifestations remain progressive. There is a potential danger in administering folic acid to patients with undiagnosed anemia since folic acid 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.

ADVERSE REACTIONS

Allergic sensitization has been reported following both oral and parenteral administration of Folic Acid.

DIRECTIONS FOR USE

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

STORAGE

Store at room temperature, USP.

To report a serious adverse event or to obtain product information, contact (888) 444-5072.

Manufactured in the USA for:
Seyer Pharmatec, Inc.
Caguas, Puerto Rico 00726

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

HEALTH CLAIM

Dietary Supplement

EZY-DOSE TABLETS

Packaging

INGREDIENTS AND APPEARANCE

HEMATRON-AF 
ascorbic acid, dl-alpha tocopheryl acetate, l-5-methyltetrahydrofolate calcium, cyanocobalamin, biotin, carbonyl iron, cupric sulfate tablet

Product Information
Product Type	DIETARY SUPPLEMENT	Item Code (Source)	NHRIC:11026-2761
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASCORBIC ACID (UNII: PQ6CK8PD0R) (ASCORBIC ACID - UNII:PQ6CK8PD0R)	ASCORBIC ACID	500 mg
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8) (.ALPHA.-TOCOPHEROL, DL- - UNII:7QWA1RIO01)	.ALPHA.-TOCOPHEROL, DL-	13.5 mg
LEVOMEFOLATE CALCIUM (UNII: A9R10K3F2F) (LEVOMEFOLIC ACID - UNII:8S95DH25XC)	LEVOMEFOLATE CALCIUM	600 ug
CYANOCOBALAMIN (UNII: P6YC3EG204) (CYANOCOBALAMIN - UNII:P6YC3EG204)	CYANOCOBALAMIN	60 ug
BIOTIN (UNII: 6SO6U10H04) (BIOTIN - UNII:6SO6U10H04)	BIOTIN	150 ug
IRON (UNII: E1UOL152H7) (IRON - UNII:E1UOL152H7)	IRON	150 mg
CUPRIC SULFATE (UNII: LRX7AJ16DT) (CUPRIC CATION - UNII:8CBV67279L)	CUPRIC CATION	3 mg

Inactive Ingredients
Ingredient Name	Strength
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
STEARIC ACID (UNII: 4ELV7Z65AP)
ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J)
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
MAGNESIUM STEARATE (UNII: 70097M6I30)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
STARCH, RICE (UNII: 4DGK8B7I3S)
ANHYDROUS DEXTROSE (UNII: 5SL0G7R0OK)
CALCIUM CARBONATE (UNII: H0G9379FGK)
CROSPOVIDONE, UNSPECIFIED (UNII: 2S7830E561)
ISOMALT (UNII: S870P55O2W)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
SUCROSE (UNII: C151H8M554)
SOYBEAN COTYLEDON CELL WALL POLYSACCHARIDES (UNII: 4UL6DF56YQ)
GLYCERIN (UNII: PDC6A3C0OX)
MINERAL OIL (UNII: T5L8T28FGP)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
ANNATTO (UNII: 6PQP1V1B6O)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
TRICALCIUM PHOSPHATE (UNII: K4C08XP666)
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
TALC (UNII: 7SEV7J4R1U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NHRIC:11026-2761-9	90 in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
dietary supplement		06/01/2024

Supplement Facts
Serving Size :		Serving per Container :
	Amount Per Serving	% Daily Value
color
shape
size (solid drugs)	21 mm
scoring	3
imprint
flavor

Labeler - Seyer Pharmatec, Inc. (832947126)