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الرئيسية / Registered in Nigeria / Vixa Daytime Caplet

Vixa Daytime Caplet

NAFDAC Reg. No. A4-100368 · Drug

Registered with NAFDAC. Registration activeAs of 4 November 2026 · synced automatically from official sources.
Product
Vixa Daytime Caplet
رقم NAFDAC
A4-100368
المادة الفعالة
Dextromethorphan; Phenylephrine Hydrochloride; Guaifenesin; Acetaminophen
التركيز
10mg; 5mg; 200mg; 325mg
الشكل
Caplet
حجم العبوة
2 x 10's
Manufacturer
Not listed
Applicant (holder)
Vixa Pharmaceutical Company Limited
Approved
26 Apr 2023
الحالة
Active View on NAFDAC ↗
التسجيل ساري حتى
25 Apr 2028
تنبيهات منظمة الصحة العالمية
None found
Community reports
None
Times checked
0

About the medicine: Dextromethorphan: uses, dosage and brands worldwide

What we found

  • Vixa Daytime Caplet is on the NAFDAC register with an active registration (A4-100368). 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. This is not medical advice. Always follow your doctor or pharmacist.

How to use Vixa Daytime Caplet

ما تقوله النشرة الرسمية. إذا وصفه لك طبيب، فاتبع الوصفة. وإذا اختلفت نشرة عبوتك، فالأولوية لها.

لمن هو

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

كيف يُتناول وكم مرة
  • 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 years of age 2.5 mL every 12 hours, not to exceed 5 mL in 24 hours
  • Children under 4 years of age do not use
Talk to a doctor first if

chronic cough that lasts such as occurs with smoking, asthma, or emphysema cough that occurs with too much phlegm (mucus)

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. …

الآثار الجانبية المحتملة

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 and breastfeeding

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

How to store it

Each 5 mL contains: sodium 7 mg store at 20-25°C (68-77°F) dosing cup provided Keep out of reach of children.

إذا نسيت جرعة

تناولها عندما تتذكر، إلا إذا اقترب موعد الجرعة التالية. عندها تخطَّ الجرعة المنسية. لا تتناول جرعتين معًا أبدًا للتعويض. راجع النشرة، فبعض الأدوية مختلفة.

From the official U.S. FDA label for this active ingredient. Your pack may have a different strength, so always read its leaflet. If a doctor prescribed it, follow the prescription. Ask a pharmacist if you are unsure. Label dated 2026-05-27.

Label for dextromethorphan and phenylephrine hydrochloride and guaifenesin and acetaminophen, the active ingredient registered with NAFDAC.

Check your pack of Vixa Daytime Caplet

Add the expiry date on your pack for a full Trust Score.

أو التقط صورًا للعبوة
تبقّت 3 عمليات تحقق مجانية اليوم Official sources: U.S. FDA · EMA (EU) · Health Canada · WHO alerts

About Vixa Daytime Caplet

What is in Vixa Daytime Caplet?

Vixa Daytime Caplet contains Dextromethorphan; Phenylephrine Hydrochloride; Guaifenesin; Acetaminophen (10mg; 5mg; 200mg; 325mg), as caplet, according to its NAFDAC registration record.

Is Vixa Daytime Caplet registered with NAFDAC?

Yes. Vixa Daytime Caplet is listed on the NAFDAC register under registration number A4-100368, and its registration is active as of 4 November 2026.

Has Vixa Daytime Caplet been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Vixa Daytime Caplet in our automatically synced alert list.

How can I check that my pack of Vixa Daytime Caplet is genuine?

Run a free authenticity scan with the NAFDAC number A4-100368, 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.

How do I take Vixa Daytime Caplet?

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…

What is Vixa Daytime Caplet 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 and phenylephrine hydrochloride and guaifenesin and acetaminophen. Always follow your doctor or pharmacist.)

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