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Klinkof Adult Syrup

NAFDAC Reg. No. C4-1856 · Drug

Registered with NAFDAC — registration activeAs of 5 November 2026 · synced automatically from official sources.
Product
Klinkof Adult Syrup
NAFDAC number
C4-1856
Active ingredient
Dextromethorphan Hydrobromide; Guaifenesin; Chlorpheniramine Maleate; Ammonium Chloride
Strength
5 mg/5 mL; 50 mg/5 mL; 2.5 mg/5 mL; 60 mg/5 mL
Form
Syrup
Pack size
1 x 100 mL
Manufacturer
Not listed
Applicant (holder)
Suitelife Pharmaceuticals Ltd
Approved
28 Sep 2021
Status
Inactive View on NAFDAC ↗
Registration valid to
27 Sep 2026
WHO alerts
None found
Community reports
None
Times checked
0

RxVerify commentary

  • Klinkof Adult Syrup is on the NAFDAC register with an active registration (C4-1856). 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 Klinkof Adult Syrup is used for

From the official U.S. FDA label for dextromethorphan hydrobromide, the active ingredient registered with NAFDAC.

What it is used for

temporarily: ■ relieves cough due to minor throat and bronchial irritation as may occur with the common cold or inhaled irritants ■ helps reduce the intensity of coughing

Purpose

Dextromethorphan HBr 5 mg: Cough suppressant

Warnings

Do Not Use ■ if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson’s disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product. Ask a doctor before use if you have ■ persistent or chronic cough such as occurs with smoking, asthma, or emphysema ■ cough that occurs with too much phlegm (mucus) Stop use and ask a doctor if cough lasts more than 7 days, comes back, or occurs with fever, rash, or persistent headache. These could be signs of a serious condition. …

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

Check your pack of Klinkof Adult Syrup

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 Klinkof Adult Syrup

What is in Klinkof Adult Syrup?

Klinkof Adult Syrup contains Dextromethorphan Hydrobromide; Guaifenesin; Chlorpheniramine Maleate; Ammonium Chloride (5 mg/5 mL; 50 mg/5 mL; 2.5 mg/5 mL; 60 mg/5 mL), as syrup, according to its NAFDAC registration record.

Is Klinkof Adult Syrup registered with NAFDAC?

Yes. Klinkof Adult Syrup is listed on the NAFDAC register under registration number C4-1856, and its registration is active as of 5 November 2026.

Has Klinkof Adult Syrup been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Klinkof Adult Syrup in our automatically synced alert list.

How can I check that my pack of Klinkof Adult Syrup is genuine?

Run a free authenticity scan with the NAFDAC number C4-1856, 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 Klinkof Adult Syrup used for?

temporarily: ■ relieves cough due to minor throat and bronchial irritation as may occur with the common cold or inhaled irritants ■ helps reduce the intensity of coughing (Summarised from the official U.S. FDA label for dextromethorphan hydrobromide. Always follow your doctor or pharmacist.)

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Reviews are personal experiences from RxVerify users, not medical advice. Report side effects to your doctor and to NAFDAC.