Dietary Supplement Label Database

Ferrocite Tablets

On market
Photo of the Breckenridge Pharmaceutical Ferrocite Tablets label
Photo of the label, from the NIH's original record · Open full size ↗
Supplement Facts
Serving Size 1 Tablet(s)
Servings Per Container 100
Amount Per Serving% Daily Value
IronIron (Form: from 324 mg of Ferrous Fumarate)106 mg588%

Other ingredients: Microcrystalline Cellulose, Citric Acid, Croscarmellose Sodium, Stearic Acid, Magnesium Stearate, Hypromellose, Titanium Dioxide, Triacetin, Mineral Oil, FD&C Yellow #5 Lake, Sodium Lauryl Sulfate, FD&C Blue No.1 Lake

% Daily Values for: Adults and children 4 or more years of age.

Where this label comes from

An original label of the NIH's Dietary Supplement Label Database, entered there on 23 July 2020, shown here as it was entered. The NIH's record

General information

Product name
Ferrocite Tablets
Brand
Breckenridge Pharmaceutical
Barcode (UPC)
3 51991 18142 2
Net contents
100 Tablet(s); 4 Blister Card(s)
Market status
On market
DSLD ID
230128

Classification

Supplement form
Tablet or Pill
Product type
Mineral
Claim types on the label
Nutrient, All Other, Structure/Function
Intended for
Adult (18 - 50 Years)

Label statements

Precautions: Allergies: Contains FD&C Yellow No. 5 Lake (Tartrazine) as a color additive (see Precautions).

Precautions: All Other: Warning: Do not exceed recommended dosage. The dietary supplementation of any anemic condition should be under the advice and supervision of a physician. Since oral iron products interfere with absorption of certain antibiotics, these products should not be taken within two hours of each other. Gastrointestinal disturbance (anorexia, nausea, diarrhea, constipation) occur occasionally, but are usually mild and subside with continuation of therapy.

Precautions: Pregnant or Nursing or Prescription Medications: Consult your doctor before use if you have, or have had, any health condition or if you are taking any medications (prescription or OTC).

Directions: Indication: For the dietary supplementation of iron deficiencies.

Precautions: Allergies: Precautions This product contains FD&C Yellow No. 5 Lake (tartrazine) which may cause allergic-type reactions (including bronchial asthma) in certain susceptible persons. Although the overall incidence of FD&C Yellow No. 5 Lake (tartrazine) sensitivity in the general population is low, it is frequently seen in patients who also have aspirin hypersensitivity.

Precautions: Pregnant or Nursing or Prescription Medications: If pregnant, or planning to become pregnant or are currently breast-feeding, please contact your physician, or health-care provider before using or continuing use.

Directions: Dosage and Administration Usual adult dosage is one tablet daily, between meals, or as directed by a physician or health-care provider. Do not exceed recommended dosage. Do not administer to children.

Precautions: All Other: Do not exceed recommended dosage.

Precautions: Children: Do not administer to children. Warning: Keep this and all medications out of the reach of children.

Storage: Storage: Store at 25 degrees C (77 degrees F); excursions permitted to 15 degrees - 30 degrees C (59 degrees - 86 degrees F). See USP Controlled Room Temperature. Protect from light and moisture.

Precautions: All Other: Warning: Cancer and Reproductive Harm - www.P65Warnings.ca.gov

Precautions: Children: 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.

Formula: Contains: Iron (from 324 mg as Ferrous Fumarate)

Precautions: All Other: Do not use if blister seals are broken

FDA Statement of Identity: Dietary Supplement

Precautions: All Other: To report a serious adverse event contact: 1-800-367-3395.

Brand information

Manufactured by: Contract Pharmacal Corp., Hauppauge, NY, USA

Distributed by: Breckenridge Pharmaceutical, Inc., Berlin, CT

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