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Rotarix Oral Suspension Tube

NAFDAC Reg. No. A6-0458 · Drug

Registered with NAFDAC — registration activeAs of 6 November 2026 · synced automatically from official sources.
Product
Rotarix Oral Suspension Tube
NAFDAC number
A6-0458
Active ingredient
Rotavirus vaccine (live, oral, monovalent)
Strength
see Composition
Form
Suspension
Pack size
1.5 mL x 1 x 50's (in squeezable LDPE tubes)
Manufacturer
Not listed
Applicant (holder)
GlaxoSmithKline Consumer Nigeria PLC (GSK)
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

RxVerify commentary

  • Rotarix Oral Suspension Tube is on the NAFDAC register with an active registration (A6-0458). 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 Rotarix Oral Suspension Tube is used for

From the official U.S. FDA label for rotavirus vaccine (live, the active ingredient registered with NAFDAC.

What it is used for

Temporarily relieves symptoms of runny nose, fever & cough.**

Purpose

Temporarily relieves symptoms of runny nose, fever & cough.**

Warnings

IF PREGNANT OR BREAST-FEEDING , ask a health care professional before use. KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away. Do not use if TAMPER EVIDENT seal is broken or missing.

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

Check your pack of Rotarix Oral Suspension Tube

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 Rotarix Oral Suspension Tube

What is in Rotarix Oral Suspension Tube?

Rotarix Oral Suspension Tube contains Rotavirus vaccine (live, oral, monovalent) (see Composition), as suspension, according to its NAFDAC registration record.

Is Rotarix Oral Suspension Tube registered with NAFDAC?

Yes. Rotarix Oral Suspension Tube is listed on the NAFDAC register under registration number A6-0458, and its registration is active as of 6 November 2026.

Has Rotarix Oral Suspension Tube been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Rotarix Oral Suspension Tube in our automatically synced alert list.

How can I check that my pack of Rotarix Oral Suspension Tube is genuine?

Run a free authenticity scan with the NAFDAC number A6-0458, 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 Rotarix Oral Suspension Tube used for?

Temporarily relieves symptoms of runny nose, fever & cough.** (Summarised from the official U.S. FDA label for rotavirus vaccine (live. 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.