FERROUS SULFATE- ferrous sulfate 325 mg green tablet, film coated 
PD-Rx Pharmaceuticals, Inc.

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Supplement Facts

Serving Size 1 Tablet

Servings Per Container 1000

 Amount Per Serving    % Daily Value
 Iron (as ferrous sulfate) 65 mg361%

Other ingredients: croscarmellose sodium, dicalcium phosphate, FD&C blue #1, FD&C yellow #6, hypromellose, magnesium stearate, microcrystalline cellulose, mineral oil, polyethylene glycol, sodium starch glycolate, stearic acid, talc, titanium dioxide, triacetin

Formula: Each tablet contains 202 mg of dried ferrous sulfate USP (65 mg of elemental iron), equivalent to 325 mg of ferrous sulfate USP.

Directions:

Adults and children over 12 years age: 1 tablet daily preferably with a meal or as directed by a doctor. Children under 12 years of age: consult a doctor. Do not exceed recommended dosage.

Caution:

Since oral iron products interfere with absorption of certain antibiotics; these products should not be taken within two hours of each other. if you are pregnant, nursing or taking any medications, consult your doctior befoe use. Discontinue use and consult your doctor if any adverse reactions occur. 

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

Store at room temperature. Keep tightly closed in a cool dry place.

Questions or comments? (866) 562-2756 Mon-Fri 8 AM to 4 PM EST

*Compare to the active ingredient in Feosol®

Ferrous 

Sulfate

Iron Supplement

325 mg

43063990 Label

FERROUS SULFATE 
ferrous sulfate 325 mg green tablet, film coated
Product Information
Product TypeDIETARY SUPPLEMENTItem Code (Source)NHRIC:43063-990
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
FERROUS SULFATE (UNII: 39R4TAN1VT) (FERROUS CATION - UNII:GW89581OWR) FERROUS CATION65 mg
Inactive Ingredients
Ingredient NameStrength
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: L11K75P92J)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
MINERAL OIL (UNII: T5L8T28FGP)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
TALC (UNII: 7SEV7J4R1U)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
TRIACETIN (UNII: XHX3C3X673)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NHRIC:43063-990-9090 in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
dietary supplement07/22/2019
Supplement Facts
Serving Size : Serving per Container :
Amount Per Serving% Daily Value
color
scoring1
shape
size (solid drugs)10 mm
Labeler - PD-Rx Pharmaceuticals, Inc. (156893695)
Registrant - PD-Rx Pharmaceuticals, Inc. (156893695)
Establishment
NameAddressID/FEIBusiness Operations
PD-Rx Pharmaceuticals, Inc.156893695repack(43063-990)

Revised: 7/2019
Document Id: 7cbd39f8-aac8-4b4f-a707-dda3a80040bc
Set id: 5599f519-766c-4f34-84cf-d314d0a550aa
Version: 1
Effective Time: 20190723
 
PD-Rx Pharmaceuticals, Inc.