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.
From the official U.S. FDA label for varicella-zoster vaccine, the active ingredient registered with NAFDAC.
Temporarily relieves symptoms of runny nose, fever & cough.**
Temporarily relieves symptoms of runny nose, fever & cough.**
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.
Add the expiry date on your pack for a full Trust Score.
Varilrix Vaccine contains Varicella-zoster vaccine, Live attenuated (0.5 mL), as powder for injection, according to its NAFDAC registration record.
Yes. Varilrix Vaccine is listed on the NAFDAC register under registration number A6-0191, and its registration is active as of 27 October 2026.
No WHO falsified or substandard medical product alert currently matches Varilrix Vaccine in our automatically synced alert list.
Run a free authenticity scan with the NAFDAC number A6-0191, 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.
Temporarily relieves symptoms of runny nose, fever & cough.** (Summarised from the official U.S. FDA label for varicella-zoster vaccine. 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.