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Inicio / Registrado en Nigeria / Praicon Gel_

Praicon Gel_

NAFDAC Reg. No. A4-101437 Estupefaciente

Registrado en NAFDAC. Registro activoAs of 6 November 2026 · synced automatically from official sources.
Producto
Praicon Gel_
Número NAFDAC
A4-101437
Principio activo
Silicon Dioxide
Dosis
10 mg
Forma
Gel
Tamaño del envase
1 x 15 g (in tube)
Fabricante
No Constan
Solicitante (titular)
Praipec Pharmaceutical Ltd
Approved
30 Jul 2025
Estado
Activo Ver en NAFDAC ↗
Registro válido hasta
29 Jul 2030
Alertas de la OMS
No se ha encontrado ninguno
Informes de la comunidad
Ninguno
Tiempos comprobados
0

Pero sobre el medicamento, Silicon dioxide: uses, dosage and brands worldwide

Lo que encontramos

  • Praicon Gel_ is on the NAFDAC register with an active registration (A4-101437). 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.

Generado automáticamente a partir del registro NAFDAC, QUIÉN alerta y los datos de la comunidad a partir de hoy. Este no es un consejo médico. Siga siempre a su médico o farmacéutico.

How to use Praicon Gel_

Lo que dice el prospecto oficial. Si te lo recetó un médico, sigue la receta. Si el prospecto de tu caja es distinto, manda el de tu caja.

Para quién es

Condition listed above or as directed by a physician.

Cómo tomarlo y con qué frecuencia

(adults/children) Dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a physician.

Talk to a doctor first if

if pellet-dispenser seal is broken.

Warnings

Stop use and ask a physician if symptoms persist for more than 3 days or worsen.

Pregnancy and breastfeeding

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

Si olvidas una dosis

Tómala en cuanto te acuerdes, salvo que falte poco para la siguiente. En ese caso, sáltate la olvidada. Nunca tomes dos dosis a la vez para compensar. Revisa tu prospecto, porque algunos medicamentos son distintos.

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 2024-01-30.

Label for silicon dioxide, the active ingredient registered with NAFDAC.

Check your pack of Praicon Gel_

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

O haz fotos de la caja
Te quedan 3 verificaciones gratis hoy Official sources: U.S. FDA · EMA (EU) · Health Canada · WHO alerts

About Praicon Gel_

What is in Praicon Gel_?

Praicon Gel_ contains Silicon Dioxide (10 mg), as gel, according to its NAFDAC registration record.

Is Praicon Gel_ registered with NAFDAC?

Yes. Praicon Gel_ is listed on the NAFDAC register under registration number A4-101437, and its registration is active as of 6 November 2026.

Has Praicon Gel_ been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Praicon Gel_ in our automatically synced alert list.

How can I check that my pack of Praicon Gel_ is genuine?

Run a free authenticity scan with the NAFDAC number A4-101437, 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 Praicon Gel_?

Follow your prescription or the leaflet in your pack. The official label says: (adults/children) Dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a physician.…

What is Praicon Gel_ used for?

Condition listed above or as directed by a physician. (Summarised from the official U.S. FDA label for silicon dioxide. 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.