Ferrocite Tabletsnone

Minerals

Brand: Breckenridge Pharmaceutical

Tablet or PillMineralOn Market
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Net Contents

100 Tablet(s)

Serving Size

1 Tablet(s)

Servings Per Container

100

Supplement Form

Tablet or Pill

Bar Code (UPC/SKU)

3 51991 18142 2

Product Version

5204-05-20

Label Analysis

Objective insights generated automatically from the official DSLD label — a quick, factual read of how this product is formulated and disclosed.

1Active Ingredients

Single-ingredient formula listed in Supplement Facts.

100%Amount Transparency

Every active ingredient discloses a specific amount per serving.

1% Daily Value Coverage

1 ingredients report a %DV; 1 meet or exceed 100% DV.

This analysis is generated algorithmically from label data for educational reference only. It is not a product endorsement, ranking, or medical advice.

Supplement Facts

Serving Size: 1 Tablet(s) · 1 per day

IngredientAmount Per Serving% Daily Value
Iron106 mg588%

Not Present

Other Ingredients

Microcrystalline CelluloseCitric AcidCroscarmellose SodiumStearic AcidMagnesium StearateHypromelloseTitanium DioxideTriacetinMineral OilFD&C Yellow #5 LakeSodium Lauryl SulfateFD&C Blue No.1 Lake

Target Groups

Adult (18 - 50 Years)

Label Claims

NutrientAll OtherStructure/Function

Directions & Suggested Use

Suggested/Recommended/Usage/Directions

Indication: For the dietary supplementation of iron deficiencies.

Suggested/Recommended/Usage/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.

Warnings & Precautions

Precautions re: Allergies

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

Precautions re: 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 re: 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).

Precautions re: 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 re: 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.

Precautions re: All Other

Do not exceed recommended dosage.

Precautions re: Children

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

Precautions re: All Other

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

Precautions re: 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.

Precautions re: All Other

Do not use if blister seals are broken

Precautions re: All Other

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

Storage

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.

Formulation

Formula re: Contains

Iron (from 324 mg as Ferrous Fumarate)

FDA Statements

FDA Disclaimer Statement

These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure or prevent any disease.

FDA Statement of Identity

Dietary Supplement

Other Label Statements

General Statements: All Other Content

How Supplied Ferrocite Tablets are round, green, film-coated tablets debossed, “B181”. Supplied in boxes of 100 tablets (4 x 25). 51991-181-42

General Statements: All Other Content

All substitutions using this product shall be pursuant to state statutes as applicable. This is not an Orange Book product.

General Statements: All Other Content

Breckenridge A Towa company

General Statements: All Other Content

(4 Blister Cards with 25 Tablets each)

Manufacturer & Distributor

Manufacturer

Contract Pharmacal Corp.

135 Adams Avenue, Hauppauge, NY, 11788, USA

Distributor

Breckenridge Pharmaceutical, Inc.

Berlin, CT, 06037

Market Reference

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  • Rx Item-Ferrocite Plus 1MG FA Tab 100 By Breckenridge Pharma Gen HEMOCYTE PLUS

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  • Breckenridge Ferrex 150 Plus Capsules

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Data sourced from the U.S. National Institutes of Health, Office of Dietary Supplements Dietary Supplement Label Database (DSLD) · Label entered 2020-07-23. DSLD Label ID: 230128. This information is provided for educational reference only and is not medical advice. Always follow the product label and consult a doctor or pharmacist before use.