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D-Koff Expectorant

NAFDAC Reg. No. 04-2751 · Drug

Registered with NAFDAC — registration activeAs of 6 November 2026 · synced automatically from official sources.
Product
D-Koff Expectorant
NAFDAC number
04-2751
Active ingredient
Bromhexine; Diphenhydramine; Ammonium chloride; Sodium citrate; Menthol
Strength
4 mg/5 mL; 10 mg/5 mL; 138 mg/5 mL; 58 mg/5 mL; 1.5 mg/5 mL
Form
Syrup
Pack size
1 x 100 mL (in amber glass bottle)
Manufacturer
Not listed
Applicant (holder)
Jawa International Limited
Approved
21 Dec 2023
Status
Active View on NAFDAC ↗
Registration valid to
20 Dec 2028
WHO alerts
None found
Community reports
None
Times checked
0

RxVerify commentary

  • D-Koff Expectorant is on the NAFDAC register with an active registration (04-2751). 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 D-Koff Expectorant is used for

From the official U.S. FDA label for D-Koff Expectorant, the active ingredient registered with NAFDAC.

What it is used for

helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and helps make cough more productive.

Possible side effects

Cough lasts more than than 7 days, comes back, or occurs with fever, rash, or persistent headache. These could be signs of serious illness.

Warnings

Do not use for children under 12 years

Pregnancy & breastfeeding

If pregnant or breast-feeding , ask a health professional before use.

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

Check your pack of D-Koff Expectorant

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 D-Koff Expectorant

What is in D-Koff Expectorant?

D-Koff Expectorant contains Bromhexine; Diphenhydramine; Ammonium chloride; Sodium citrate; Menthol (4 mg/5 mL; 10 mg/5 mL; 138 mg/5 mL; 58 mg/5 mL; 1.5 mg/5 mL), as syrup, according to its NAFDAC registration record.

Is D-Koff Expectorant registered with NAFDAC?

Yes. D-Koff Expectorant is listed on the NAFDAC register under registration number 04-2751, and its registration is active as of 6 November 2026.

Has D-Koff Expectorant been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches D-Koff Expectorant in our automatically synced alert list.

How can I check that my pack of D-Koff Expectorant is genuine?

Run a free authenticity scan with the NAFDAC number 04-2751, 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 D-Koff Expectorant used for?

helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and helps make cough more productive. (Summarised from the official U.S. FDA label for D-Koff Expectorant. 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.