NAFDAC Reg.-Nr. 04-3259 Medikament
About the medicine: Bromhexine: uses, dosage and brands worldwide
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.
What the official label says. If a doctor prescribed it, follow the prescription. Your pack's leaflet comes first if it is different.
Temporarily relieves cough due to minor throat and bronchial irritation as may occur with the common cold or inhaled irritants the impulse to cough to help you get to sleep
chronic cough that lasts such as occurs with smoking, asthma, or emphysema cough that occurs with too much phlegm (mucus)
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 chronic cough that lasts 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 headache that lasts. These could be signs of a serious condition. …
Cough lasts more than 7 days, comes back, or occurs with fever, rash, or headache that lasts. These could be signs of a serious condition.
If pregnant or breast-feeding, ask a health professional before use.
Each 5 mL contains: sodium 7 mg store at 20-25°C (68-77°F) dosing cup provided Keep out of reach of children.
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.
Label for bromhexine (bromhexine hydrochloride) and dextromethorphan and ammonium chloride and menthol, the active ingredient registered with NAFDAC.
Add the expiry date on your pack for a full Trust Score.
Zedex Cough Syrup contains Bromhexine (Bromhexine Hydrochloride); Dextromethorphan; Ammonium chloride; Menthol (8 mg/5 mL; 10 mg/5 mL; 100 mg/5 mL; 5 mg/5 mL), as liquid, according to its NAFDAC registration record.
Yes. Zedex Cough Syrup is listed on the NAFDAC register under registration number 04-3259, and its registration is active as of 1 November 2026.
No WHO falsified or substandard medical product alert currently matches Zedex Cough Syrup in our automatically synced alert list.
Run a free authenticity scan with the NAFDAC number 04-3259, 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.
Follow your prescription or the leaflet in your pack. The official label says: shake bottle well before use measure only with dosing cup provided do not use dosing cup with other products dose as follows or as directed by a doctor mL = milliliter adults and children 12 years of age and over 10 mL every 12 hours, not to exceed 20 mL in 24 hours children 6 to under 12 years of age 5 mL every 12 hours, not to exceed 10 mL in 24 hours children 4 to under 6 ye…
temporarily relieves cough due to minor throat and bronchial irritation as may occur with the common cold or inhaled irritants the impulse to cough to help you get to sleep (Summarised from the official U.S. FDA label for bromhexine (bromhexine hydrochloride) and dextromethorphan and ammonium chloride and menthol. Always follow your doctor or pharmacist.)
Reviews are personal experiences from PillVera users, not medical advice. Report side effects to your doctor and to NAFDAC.