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Gida / Rijista a Najeriya / King Capsule## (strength format)

King Capsule## (strength format)

NAFDAC Reg. A'a. A4-1202 · Magungunan miyagun ƙwayoyi

Rijista tare da NAFDAC. Rijista mai aikiAs of 30 October 2026 · synced automatically from official sources.
Product
King Capsule## (strength format)
NAFDAC number
A4-1202
Active ingredient
Ferrous Fumarate; Vitamin A; Folic Acid; Cyanocobalamin; Thiamine Hydrochloride; Riboflavin; Pyridoxine Hydrochloride; Nicotinamide; Ascorbic Acid; Calcium Pantothenate; Zinc
Strength
307.7mg;1000iu; 400mcg; 4mcg; 5mg; 3mg; 2mg; 20mg; 100mg; 7mg; 5mg
Form
Capsule
Pack size
3 x 10's, 12 x 10's (in PVC-Alu blisters)
Manufacturer
Not listed
Applicant (holder)
SKG - Pharma Ltd
Approved
30 Nov 2023
Status
Active View on NAFDAC ↗
Registration valid to
29 Nov 2028
WHO alerts
None found
Community reports
None
Times checked
0

About the medicine: Ferrous fumarate: uses, dosage and brands worldwide

What we found

  • King Capsule## (strength format) is on the NAFDAC register with an active registration (A4-1202). A valid number alone does not prove a pack is genuine — counterfeiters copy real numbers, so also check the expiry date, seal and print quality.

Generated automatically from the NAFDAC register, WHO alerts and community data as of today. This is not medical advice. Always follow your doctor or pharmacist.

How to use King Capsule## (strength format)

What the official label says. If a doctor prescribed it, follow the prescription. Your pack's leaflet comes first if it is different.

Who it is for

INDICATIONS: Integra FTM is indicated for the treatment of iron deficiency anemia, and folate deficiency anemia. Integra FTM is indicated in pregnancy for the prevention and treatment of iron deficiency and to supply a maintenance dosage of folic acid.

How to take it and how often
  • Adults (persons over 12 years of age), One capsule daily, between meals, or as prescribed by a physician
  • Do not exceed recommended dosage
  • Do not administer to children under the age of 12
Children
  • Safety and effectiveness of this product have not been established
  • In pediatric patients
Older adults

No clinical studies have been performed in patients age 65 and over to determine whether older persons respond differently from younger persons. Dosage should always begin at the low end of the dosage scale and should consider that elderly persons may have decreased hepatic, renal, or cardiac function and or concomitant diseases.

Talk to a doctor first if
  • Integra FTM is contraindicated in patients with known hypersensitivity to any of its ingredients; also, all iron compounds are contraindicated in patients with hemosiderosis, hemochromatosis, or hemolytic anemias
  • Pernicious anemia is a contraindication, as folic acid may obscure its signs and symptoms
Warnings

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. WARNING: Folic acid alone is improper therapy in the treatment for pernicious anemia and other megaloblastic anemias where Vitamin B12 is deficient. PRECAUTIONS: General: Anemia is a manifestation that requires appropriate investigation to determine its cause or causes. No single regimen fits all cases and the status of the patient observed in follow-up is the final criterion for adequacy of therapy. …

Possible side effects

Folic Acid: Allergic sensitizations have been reported following both oral and parenteral administration of folic acid. Ferrous Fumarate: Gastrointestinal disturbances (anorexia, nausea, diarrhea, constipation, heartburn and vomiting) occur occasionally, but are usually mild and may subside with continuation of therapy. Reducing the dose and administering it with meals will minimize these effects in the sensitive patient. Increasing fiber in the diet can relieve constipation. Iron may turn stools black. This is a harmless effect that is a result of unabsorbed iron. Although the absorption of iron is best when taken between meals, giving Integra FTM after meals may control occasional G.I. …

Pregnancy and breastfeeding

USAGE IN PREGNANCY: Before Integra FTM is prescribed for megaloblastic anemia in pregnancy, appropriate diagnostic exclusion of Addisonian pernicious anemia, (due to faulty or blocked absorption of vitamin B12, or extrinsic factor or either a genetic, immunological or surgical basis) should be carried out.

If you take too much

OVERDOSE: Iron: Signs and Symptoms: Iron is toxic. Acute overdosage of iron may cause nausea and vomiting and, in severe cases, cardiovascular collapse and death. Other symptoms include pallor and cyanosis, melena, shock, drowsiness and coma. The estimated overdose of orally ingested iron is 300-mg/kg body weight. When overdoses are ingested by children, severe reactions, including fatalities, have resulted. Integra FTM should be stored beyond the reach of children to prevent against accidental iron poisoning. Keep this and all other drugs out of the reach of children. …

If you miss a dose

Take it when you remember, unless it is nearly time for the next dose. Then skip the missed one. Never take two doses at once to make up for it. Check your leaflet, as some medicines are different.

From the official U.S. FDA label for this active ingredient. Your pack may have a different strength, so always read its leaflet. If a doctor prescribed it, follow the prescription. Ask a pharmacist if you are unsure. Label dated 2022-11-08.

Label for ferrous fumarate and vitamin a and folic acid and cyanocobalamin and thiamine hydrochloride and riboflavin and pyridoxine hydrochloride and nicotinamide and ascorbic acid and calcium pantothenate and zinc, the active ingredient registered with NAFDAC.

NAFDAC recall & alert notices

Public Alert No. 036/2026 – Alert on Suspected Counterfeit Products Mimicking Forxiga® (Dapagliflozin) 18 Jul 2026 · nafdac.gov.ngThe National Agency for Food and Drug Administration and Control (NAFDAC) is informing the public of the detection of suspected counterfeit medicinal products found in the Nigerian market that infringe on the approved marketing authorization of Forxiga® (dapagliflozin) manufactured by AstraZeneca.AstraZeneca notified N…Public Alert No. 0035/2022 – European Rapid Alert System For Dangerous Non-Food Products: Banned Cosmetic Product-Professional Mouse Pro-Vitamin B5 By United Kingdom Studio 2000 System21 Aug 2022 · nafdac.gov.ng, The National Agency for Food and Drug Administration and Control (NAFDAC)has received safety information from European Rapid Alert System for dangerous non- food products that a cosmetic product; Professional Mouse Pro-Vitamin B5 manufactured by United Kingdom Studio 2000 system has been banned. The product contains …Public Alert No: 29/2021 – Prairie Wolf Spirits Inc. Recalls Prairie Wolf Distillery Hand Sanitizer Packed In 16.9 Oz And 20.0 Oz Bottles Resembling Drinking Water Containers10 Aug 2021 · nafdac.gov.ng, The National Agency for Food and Drug Administration and Control (NAFDAC)  has received information from US FDA on the voluntary recall by manufacturer of Prairie Wolf Distillery hand sanitizer packaged in 16.9 fluid ounce (UPC 6000331899) and 20.0 fluid ounce (UPC 6000365984) containers to the consumer level. The pr…Apotex Corp Recalls Enoxaparin Sodium Injection USP due to Mislabelling of Syringe Barrel Measurement Markings18 Feb 2021 · nafdac.gov.ng, The National Agency for Food and Drug Administration and Control (NAFDAC) has received information from the US FDA that Apotex Corp is voluntarily recalling two (2) batches of Enoxaparin Sodium Injection, USP due to a packaging error resulting in some syringes barrels containing 150 mg/mL markings (corresponding to 1…

Compare the brands and batch numbers in these notices with your pack, or enter your batch number above.

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3 free checks left today Official sources: U.S. FDA · EMA (EU) · NAFDAC · WHO alerts

About King Capsule## (strength format)

What is in King Capsule## (strength format)?

King Capsule## (strength format) contains Ferrous Fumarate; Vitamin A; Folic Acid; Cyanocobalamin; Thiamine Hydrochloride; Riboflavin; Pyridoxine Hydrochloride; Nicotinamide; Ascorbic Acid; Calcium Pantothenate; Zinc (307.7mg;1000iu; 400mcg; 4mcg; 5mg; 3mg; 2mg; 20mg; 100mg; 7mg; 5mg), as capsule, according to its NAFDAC registration record.

Is King Capsule## (strength format) registered with NAFDAC?

Yes. King Capsule## (strength format) is listed on the NAFDAC register under registration number A4-1202, and its registration is active as of 30 October 2026.

Has King Capsule## (strength format) been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches King Capsule## (strength format) in our automatically synced alert list.

How can I check that my pack of King Capsule## (strength format) is genuine?

Run a free authenticity scan with the NAFDAC number A4-1202, your pack's expiry date and batch number to get a Trust Score, compare the pack with the NAFDAC record (ingredient, strength, form, manufacturer), and buy only from licensed pharmacies.

How do I take King Capsule## (strength format)?

Follow your prescription or the leaflet in your pack. The official label says: Adults (persons over 12 years of age), One (1) capsule daily, between meals, or as prescribed by a physician. Do not exceed recommended dosage. Do not administer to children under the age of 12.…

What is King Capsule## (strength format) used for?

INDICATIONS: Integra FTM is indicated for the treatment of iron deficiency anemia, and folate deficiency anemia. Integra FTM is indicated in pregnancy for the prevention and treatment of iron deficiency and to supply a maintenance dosage of folic acid. (Summarised from the official U.S. FDA label for ferrous fumarate and vitamin a and folic acid and cyanocobalamin and thiamine hydrochloride and riboflavin and pyridoxine hydrochloride and nicotinamide and ascorbic acid and calcium pantothenate and zinc. Always follow your doctor or pharmacist.)

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