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Rotaflu Tablet## (strength format)

NAFDAC Reg. No. A4-100697 · Drug

Registered with NAFDAC. Registration activeAs of 28 October 2026 · synced automatically from official sources.
Product
Rotaflu Tablet## (strength format)
NAFDAC number
A4-100697
Active ingredient
Loratadine; Pseudoephedrine HCl
Strength
5mg; 120mg
Form
Tablet
Pack size
1 x 10's (in blister)
Manufacturer
Not listed
Applicant (holder)
Rotamedics Pharmacy Limited
Approved
31 Jan 2024
Status
Active View on NAFDAC ↗
Registration valid to
30 Jan 2029
WHO alerts
None found
Community reports
None
Times checked
0

What we found

  • Rotaflu Tablet## (strength format) is on the NAFDAC register with an active registration (A4-100697). 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 Rotaflu Tablet## (strength format)

What the official label says. If a doctor prescribed it, follow the prescription. Your pack's leaflet comes first if it is different.

Who it is for

temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: • runny nose • itchy, watery eyes • sneezing • itching of the nose or throat

How to take it and how often
  • Adults and
  • Children 6 years and over 1 tablet daily; not more than 1 tablet in 24 hours
  • Children under 6 years of age
  • Ask a doctor consumers with liver or kidney disease
  • Ask a doctor
While you are taking it
  • Do not take more than directed
  • Taking more than directed may cause drowsiness
Talk to a doctor first if
  • Liver or kidney disease
  • Your doctor should determine if you need a different dose
Warnings

Do not use if you have ever had an allergic reaction to this product or any of its ingredients Ask a doctor before use if you have liver or kidney disease. Your doctor should determine if you need a different dose. When using this product do not take more than directed. Taking more than directed may cause drowsiness. Stop use and ask a doctor if an allergic reaction to this product occurs. Seek medical help right away. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

Possible side effects

an allergic reaction to this product occurs. Seek medical help right away.

Pregnancy and breastfeeding

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

How to store it

• do not use if printed foil under cap is broken or missing • store between 20 ° to 25 ° C (68 ° to 77 ° F) Keep out of reach of children.

If you miss a dose

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.

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 2026-02-25.

Label for loratadine and pseudoephedrine hcl, the active ingredient registered with NAFDAC.

Check your pack of Rotaflu Tablet## (strength format)

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

3 free checks left today Official sources: NAFDAC · WHO · U.S. FDA · Health Canada · NLM

About Rotaflu Tablet## (strength format)

What is in Rotaflu Tablet## (strength format)?

Rotaflu Tablet## (strength format) contains Loratadine; Pseudoephedrine HCl (5mg; 120mg), as tablet, according to its NAFDAC registration record.

Is Rotaflu Tablet## (strength format) registered with NAFDAC?

Yes. Rotaflu Tablet## (strength format) is listed on the NAFDAC register under registration number A4-100697, and its registration is active as of 28 October 2026.

Has Rotaflu Tablet## (strength format) been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Rotaflu Tablet## (strength format) in our automatically synced alert list.

How can I check that my pack of Rotaflu Tablet## (strength format) is genuine?

Run a free authenticity scan with the NAFDAC number A4-100697, 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 Rotaflu Tablet## (strength format)?

Follow your prescription or the leaflet in your pack. The official label says: adults and children 6 years and over 1 tablet daily; not more than 1 tablet in 24 hours children under 6 years of age ask a doctor consumers with liver or kidney disease ask a doctor…

What is Rotaflu Tablet## (strength format) used for?

temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: • runny nose • itchy, watery eyes • sneezing • itching of the nose or throat (Summarised from the official U.S. FDA label for loratadine and pseudoephedrine hcl. 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.