Ferrous Gluconate - A-S Medication Solutions

Manufacturer
A-S Medication Solutions
Effective date
2026-08-19
Label type
DIETARY SUPPLEMENT
Version
14
Source
daily-update
Hydrated at
2026-08-21 02:02:30

Label at a glance#

ProductFerrous Gluconate
Active ingredientFERROUS GLUCONATE
Label structure6 sections

Label contents#

Full prescribing information#

STATEMENT OF IDENTITY SECTION

Dietary Supplement

WARNINGS SECTION

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.

WARNINGS:

WARNINGS SECTION

Do not take within 2 hours of taking oral tetracycline antibiotics, since oral iron products tend to interfere with absorption of tetracycline. May cause gastrointestinal discomfort, nausea, constipation or diarrhea. If you are pregnant or nursing a baby, seek advice of a health professional before using this product. U.S. Consumer Product Safety Commission requires that iron-containing medicines and vitamins with iron be packaged in child-resistant closures. Parents should always properly resecure safety closures.

STORAGE:

SAFE HANDLING WARNING SECTION

Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature]

Supplement Facts

DOSAGE & ADMINISTRATION SECTION

Serving Size 1 Tablet
Amount Per Tablet% Daily Value

Iron (as ferrous gluconate) 38 mg

208%

Other ingredients: Colloidal Silicon Dioxide, Corn Starch, Talc, Powdered Cellulose, Sodium Starch Glycolate, Stearic Acid, Titanium Dioxide, Polyethylene Glycol, Sucrose, Calcium Carbonate, Magnesium Stearate, Copovidone, Shellac, Cocoa Butter, FD&C Blue No. 1 Aluminum Lake, Maltodextrin, Hypromellose, Riboflavin, Carnauba Wax, White Wax.

Distributed by Padagis®
Minneapolis, MN 55427

02-23

FERROUS GLUCONATE TABLET

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label Image
Label Image

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeData Matrix(01)00350090026901(17)991231(10)9987654(21)AA000000lbl500900269.jpg

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-0269-0EA - Each50090-02693b60ccb5-7f76-4cfa-9521-5914000ded5712024-01-04
50090-0269-2EA - Each50090-02692f3369df-7f0b-4063-84e1-3d6cb687750612024-01-04
50090-0269-3EA - Each50090-0269ccffc22f-48b3-4334-b2b6-bddf589c63b012024-01-04
0574-0508-01EA - Each0574-05081f3c7fb5-421d-40f6-b2ed-08d071d1b96d12013-02-19
0574-0508-10EA - Each0574-0508ec8a1bcb-34f1-4ccd-8bf2-23ee13c8ae5a12013-02-19
0574-0508-11EA - Each0574-0508e61e310a-9754-4a3a-9829-c63ca492994f12013-02-19

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50090-026950090-0269-3, 50090-0269-2, 50090-0269-0
0574-0508

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 19 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
122026-08-13daily-update2026-08-18 02:03:39
92025-01-06full-release2026-06-01 02:51:23

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.