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Vixa Night-Time Relief Caplet## (strength format)

NAFDAC Reg. No. A4-100369 · Drug

Registered with NAFDAC — registration activeAs of 5 November 2026 · synced automatically from official sources.
Product
Vixa Night-Time Relief Caplet## (strength format)
NAFDAC number
A4-100369
Active ingredient
Dextromethorphan; Phenylephrine Hydrochloride; Doxylamine Succinate; Acetaminophen
Strength
10mg; 5mg; 6.25mg; 325mg
Form
Caplet
Pack size
2 x 10's
Manufacturer
Not listed
Applicant (holder)
Vixa Pharmaceutical Company Limited
Approved
26 Apr 2023
Status
Active View on NAFDAC ↗
Registration valid to
25 Apr 2028
WHO alerts
None found
Community reports
None
Times checked
0

RxVerify commentary

  • Vixa Night-Time Relief Caplet## (strength format) is on the NAFDAC register with an active registration (A4-100369). 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 Vixa Night-Time Relief Caplet## (strength format) is used for

From the official U.S. FDA label for dextromethorphan, 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 the impulse to cough to help you get to sleep

Purpose

Cough suppressant

Possible side effects

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.

Do not use if

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.

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 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. …

Pregnancy & breastfeeding

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

Storage

each 5 mL contains: sodium 7 mg store at 20-25°C (68-77°F) dosing cup provided

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

Check your pack of Vixa Night-Time Relief Caplet## (strength format)

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 Vixa Night-Time Relief Caplet## (strength format)

What is in Vixa Night-Time Relief Caplet## (strength format)?

Vixa Night-Time Relief Caplet## (strength format) contains Dextromethorphan; Phenylephrine Hydrochloride; Doxylamine Succinate; Acetaminophen (10mg; 5mg; 6.25mg; 325mg), as caplet, according to its NAFDAC registration record.

Is Vixa Night-Time Relief Caplet## (strength format) registered with NAFDAC?

Yes. Vixa Night-Time Relief Caplet## (strength format) is listed on the NAFDAC register under registration number A4-100369, and its registration is active as of 5 November 2026.

Has Vixa Night-Time Relief Caplet## (strength format) been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Vixa Night-Time Relief Caplet## (strength format) in our automatically synced alert list.

How can I check that my pack of Vixa Night-Time Relief Caplet## (strength format) is genuine?

Run a free authenticity scan with the NAFDAC number A4-100369, 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 Vixa Night-Time Relief Caplet## (strength format) used for?

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 dextromethorphan. 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.