HEMOCYTE F- folic acid and iron tablet

Hemocyte F by

Drug Labeling and Warnings

Hemocyte F 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*	% Daily value for Pregnant or lactating woman
Folic acid	1000 mcg	250%	125 %
Iron( from Ferrous Fumarate)	106 mg	589 %	589 %
* percent daily value based on 2,000 calorie diet

STATEMENT OF IDENTITY

Iron/Folic acid Supplement 

WARNINGS

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.

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

1 tablet daily, between meals, orally,

Do not exceed recommended dosage. Do not administer to children

Product information: Physician's complete prescribing information is found printed inside carton. Do not purchase if any portion of product is opened.

HEALTH CLAIM

Iron/Folic acid Supplement

Packaging

INGREDIENTS AND APPEARANCE

HEMOCYTE F 
folic acid and iron tablet

Product Information
Product Type	DIETARY SUPPLEMENT	Item Code (Source)	NHRIC:52747-306
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
FOLIC ACID (UNII: 935E97BOY8) (FOLIC ACID - UNII:935E97BOY8)	FOLIC ACID	1 mg
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)
POLYVINYL ALCOHOL (UNII: 532B59J990)
MAGNESIUM STEARATE (UNII: 70097M6I30)
POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
FD&C RED NO. 40 (UNII: WZB9127XOA)
TALC (UNII: 7SEV7J4R1U)
HYPROMELLOSES (UNII: 3NXW29V3WO)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NHRIC:52747-306-30	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(52747-306)