Drug Facts:

Active Ingredient
(in each tablet): Purpose:

160 mg dried ferrous sulfate,
USP (equivalent to 50 mg
elemental iron) Iron deficiency

Uses: For use in the prevention of iron deficiency when the need for such therapy has been determined by a doctor.

Warnings:

The treatment of any anemic condition should be under the advice and supervision of a doctor.
As oral iron products interfere with absorption of oral tetracycline antibiotics, these products should not be taken within two hours of each other.
If pregnant or breast-feeding, ask a health professional before use.

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.

Directions:

Tablets must be swallowed whole.
ADULTS: One or two tablets daily or as recommended by a doctor. A maximum of four tablets daily may be taken.
CHILDREN UNDER 12: consult a doctor

Other Information:

store at controlled room temperature 20-25°C (68-77°F)
protect from moisture

Inactive Ingredients: cetostearyl alcohol, FD&C blue #2 aluminum lake, hypromellose, lactose, magnesium stearate, polysorbate 80, talc, titanium dioxide, yellow iron oxide

Questions? call 1-800-452-0051 24 hours a day, 7 days a week.

How Supplied: Child-resistant blister packages of 30 ct., 60 ct. and 90 ct. NDC 0067-0125-47.

Child Resistant

Blister packaged for your protection.

Do not use if individual seals are broken.

Tablets non-USP (disintegration, content uniformity)

Tablets made in Great Britain

PRODUCT PHOTO(S):

NOTE: These photos can be used only for identification by shape, color, and imprint. They do not depict actual or relative size.

The product samples shown here have been supplied by the manufacturer and reproduced in full color by PDR as a quick-reference identification aid. While every effort has been made to assure accurate reproduction, please remember that any visual identification should be considered preliminary. In cases of poisoning or suspected overdosage, the drug's identity should be verified by chemical analysis.