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King Tonic## (strength format, check dosage form)

NAFDAC Reg. No. 04-2326 · Drug

Registered with NAFDAC — registration activeAs of 6 November 2026 · synced automatically from official sources.
Product
King Tonic## (strength format, check dosage form)
NAFDAC number
04-2326
Active ingredient
Ferrous Fumarate; Thiamine Hydrochloride; Riboflavin; Pyridoxine Hydrochloride; Nicotinamide; Calcium D-Pantothenate; Vitamin B12
Strength
45.539mg/5ml; 3.5mg/5ml; 1mg/5ml; 2mg/5ml; 15mg/5ml; 6mg/5ml; 2mcg/5ml
Form
Liquid
Pack size
1 x 200 mL (in amber bottle)
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

RxVerify commentary

  • King Tonic## (strength format, check dosage form) is on the NAFDAC register with an active registration (04-2326). 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. Not medical advice — always follow your doctor or pharmacist.

What King Tonic## (strength format, check dosage form) is used for

From the official U.S. FDA label for ferrous fumarate, the active ingredient registered with NAFDAC.

What it is 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.

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. …

Do not use 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. …

Pregnancy & 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.

General information only — not dosing advice. Always follow the leaflet in your pack and your doctor or pharmacist.

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…

Notices list affected brands and batch numbers — compare them with your pack. Enter your batch number above to check it automatically.

Check your pack of King Tonic## (strength format, check dosage form)

Add the expiry date printed on your pack for a full Trust Score — or look up uses, side effects and cheaper generics.

3 free checks left today · no signup Official sources: NAFDAC Green Book & recalls · WHO · U.S. FDA · NLM RxNorm

About King Tonic## (strength format, check dosage form)

What is in King Tonic## (strength format, check dosage form)?

King Tonic## (strength format, check dosage form) contains Ferrous Fumarate; Thiamine Hydrochloride; Riboflavin; Pyridoxine Hydrochloride; Nicotinamide; Calcium D-Pantothenate; Vitamin B12 (45.539mg/5ml; 3.5mg/5ml; 1mg/5ml; 2mg/5ml; 15mg/5ml; 6mg/5ml; 2mcg/5ml), as liquid, according to its NAFDAC registration record.

Is King Tonic## (strength format, check dosage form) registered with NAFDAC?

Yes. King Tonic## (strength format, check dosage form) is listed on the NAFDAC register under registration number 04-2326, and its registration is active as of 6 November 2026.

Has King Tonic## (strength format, check dosage form) been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches King Tonic## (strength format, check dosage form) in our automatically synced alert list.

How can I check that my pack of King Tonic## (strength format, check dosage form) is genuine?

Run a free authenticity scan with the NAFDAC number 04-2326, 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.

What is King Tonic## (strength format, check dosage form) 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. Always follow your doctor or pharmacist.)

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