Hemocyte by US Pharmaceutical Corporation / PD SUB, LLC. HEMOCYTE- iron tablet

Hemocyte by

Drug Labeling and Warnings

Hemocyte by is a Other medication manufactured, distributed, or labeled by US Pharmaceutical Corporation, PD SUB, LLC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

STATEMENT OF IDENTITY

Supplement Facts
Serving Size: 1 Tablet
Amount per Serving		* % DV
Iron( from ferrous fumarate)	106 mg	588.9 %
* Percent daily value based on 2,000 calorie diet

Indications

A hematinic supplement for iron deficiency for anemia

SIDE EFFECTS: Gastrointestinal disturbances (anorexia, nausea, diarrhea, constipation) occur occasionally but are usually mild and subside with continuation of therapy.

WARNING

WARNING: Accidental overdose of iron-containing products is a leading cause of fatal poisoning in children under 6. Keep this product out of reach of children. In case of accidental overdose, call a doctor or poison control center immediately.

If you are  pregnant or nursing a baby, seek the advice of a health professional before using the product.

Do not purchase if any portion of product is opened.

PRECAUTIONS

You should contact your healthcare provider for medical advice about adverse events. To report a serious adverse event, contact US Pharmaceutical Corporation, P.O Box 360465, Decatur,GA 30036

SAFE HANDLING WARNING

Store at controlled room temperature between 15°-30°C (59°-86 °F ). Keep in a cool ,dry place. Capsules are not USP

DOSAGE & ADMINISTRATION

DOSAGE:Adults (persons over 12 years of age), one (1) tablet daily, between meals, or as prescribed by a physician. Do not exceed recommended dosage. Do not administer to children under the age of 12.

HOW SUPPLIED: Hemocyte is  a round, dark red film coated tablet debossed with the "US" logo on one side . Hemocyte is supplied in boxes of 30 tablets, NDC 52747-307-30 and 100 tablets, NDC 52747-307-70

HEALTH CLAIM

A hematinic supplement for iron deficiency for anemia

Packaging

INGREDIENTS AND APPEARANCE

HEMOCYTE 
iron tablet

Product Information
Product Type	DIETARY SUPPLEMENT	Item Code (Source)	NHRIC:52747-307
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
FERROUS FUMARATE (UNII: R5L488RY0Q) (FERROUS CATION - UNII:GW89581OWR)	FERROUS CATION	106 mg

Inactive Ingredients
Ingredient Name	Strength
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
MAGNESIUM STEARATE (UNII: 70097M6I30)
POLYVINYL ALCOHOL (UNII: 532B59J990)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
FD&C RED NO. 40 (UNII: WZB9127XOA)
TALC (UNII: 7SEV7J4R1U)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NHRIC:52747-307-30	3 in 1 BOX
1		10 in 1 BLISTER PACK

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
dietary supplement		10/01/1984

Supplement Facts
Serving Size :		Serving per Container :
	Amount Per Serving	% Daily Value
color
shape
size (solid drugs)	10 mm
scoring	1
imprint

Labeler - US Pharmaceutical Corporation (048318224)

Establishment
Name	Address	ID/FEI	Business Operations
PD SUB, LLC.		063753431	manufacture(52747-307)