FERROUS SULFATE tablet, delayed release

Ferrous Sulfate by

Drug Labeling and Warnings

Ferrous Sulfate by is a Other medication manufactured, distributed, or labeled by Rising Pharma Holdings, Inc., Nucrogene Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Supplement Facts

Serving size: 1 Tablet

Servings Per Container: 100 and 1,000

	Amount Per Serving	% Daily Value
Iron (as dried ferrous sulfate)	65 mg	361%

Other Ingredients: Croscarmellose sodium, dibasic calcium phosphate dihydrate, FD&C Red No. 40, hypromellose, magnesium stearate, methacrylic acid, microcrystalline cellulose, polyethylene glycol, silicon dioxide, stearic acid, titanium dioxide, triacetin.

Directions:

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

Caution:

Since oral iron products interfere with absorption of oral tetracycline antibiotics, these products should not be taken within two hours of each other. Iron-containing products may cause constipation or diarrhea. As with any dietary supplement, if you are pregnant or nursing a baby, seek the advice of a health professional before using this product.

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

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.

SAFE HANDLING WARNING

Questions or comments? call 1-844-474-7464

Distributed by:

Rising Pharma Holdings, Inc.

East Brunswick, NJ 08816

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FERROUS SULFATE 
ferrous sulfate tablet, delayed release

Product Information
Product Type	DIETARY SUPPLEMENT	Item Code (Source)	NHRIC:57237-365
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
FERROUS SULFATE (UNII: 39R4TAN1VT) (FERROUS CATION - UNII:GW89581OWR)	FERROUS CATION	65 mg

Inactive Ingredients
Ingredient Name	Strength
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)
FD&C RED NO. 40 (UNII: WZB9127XOA)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
MAGNESIUM STEARATE (UNII: 70097M6I30)
METHACRYLIC ACID (UNII: 1CS02G8656)
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
STEARIC ACID (UNII: 4ELV7Z65AP)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
TRIACETIN (UNII: XHX3C3X673)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NHRIC:57237-365-01	100 in 1 BOTTLE, PLASTIC
2	NHRIC:57237-365-10	1000 in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
dietary supplement		12/22/2025

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

FERROUS SULFATE 
ferrous sulfate tablet, delayed release

Product Information
Product Type	DIETARY SUPPLEMENT	Item Code (Source)	NHRIC:57237-366
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
FERROUS SULFATE (UNII: 39R4TAN1VT) (FERROUS CATION - UNII:GW89581OWR)	FERROUS CATION	65 mg

Inactive Ingredients
Ingredient Name	Strength
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)
FD&C RED NO. 40 (UNII: WZB9127XOA)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
MAGNESIUM STEARATE (UNII: 70097M6I30)
METHACRYLIC ACID (UNII: 1CS02G8656)
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
STEARIC ACID (UNII: 4ELV7Z65AP)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
TRIACETIN (UNII: XHX3C3X673)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NHRIC:57237-366-01	100 in 1 BOTTLE, PLASTIC
2	NHRIC:57237-366-10	1000 in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
dietary supplement		12/22/2025

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

Labeler - Rising Pharma Holdings, Inc. (116880195)

Registrant - Nucrogene Inc (110928621)

Establishment
Name	Address	ID/FEI	Business Operations
Nucrogene Inc		110928621