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Inicio / Registrado en Nigeria / Vitamin E 400 IU Soft Gel

Vitamin E 400 IU Soft Gel

NAFDAC Reg. No. A4-8322 Estupefaciente

Registrado en NAFDAC. Registro activoAs of 1 November 2026 · synced automatically from official sources.
Producto
Vitamin E 400 IU Soft Gel
Número NAFDAC
A4-8322
Principio activo
Tocopherol (vitamin E)
Dosis
440 mg
Forma
Capsule
Tamaño del envase
3 x 10's (in PVC blisters)
Fabricante
No Constan
Solicitante (titular)
Emzor Pharmaceutical Industries Limited
Approved
31 Oct 2023
Estado
Activo Ver en NAFDAC ↗
Registro válido hasta
30 Oct 2028
Alertas de la OMS
No se ha encontrado ninguno
Informes de la comunidad
Ninguno
Tiempos comprobados
0

Pero sobre el medicamento, Tocopherol: uses, dosage and brands worldwide

Lo que encontramos

  • Vitamin E 400 IU Soft Gel is on the NAFDAC register with an active registration (A4-8322). 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 Vitamin E 400 IU Soft 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.

Advertencia grave: Ingestion of more than 3 grams of omega-3 fatty acids (such as DHA) per day has been shown to have potential antithrombotic effects, including an increased bleeding time and International Normalized Ratio (INR). Administration of omega-3 fatty acids should be avoided in patients taking anticoagulants and in those known to have an inherited or acquired predisposition to bleeding. WARNING: Accidental overdose of iron-containing products is a leading cause of fatal poisoning in children under 6. …
Para quién es

INDICATIONS: PNV-DHA is a multivitamin/multimineral fatty acid dietary supplement indicated for use in improving the nutritional status of women throughout pregnancy and in the postnatal period for both lactating and nonlactating mothers.

Cómo tomarlo y con qué frecuencia

Before, during and/or after pregnancy, one softgel daily or as directed by a physician.

Talk to a doctor first if

PNV-DHA is contraindicated in patients with a known hypersensitivity to any of the ingredients.

Warnings

PRECAUTIONS: Folic acid alone is improper therapy in the treatment of pernicious anemia and other megaloblastic anemias where Vitamin B 12 is deficient. Folic acid in doses above 1.0 mg daily may obscure pernicious anemia in that hematologic remission can occur while neurological manifestations progress.

Posibles efectos secundarios

Allergic sensitization has been reported following both oral and parenteral administration of folic acid.

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 2026-07-23.

Label for tocopherol (vitamin e), the active ingredient registered with NAFDAC.

NAFDAC recall & alert notices

Public Alert No. 023/2025 – Recall of Multivitamin Supplements due to Risk of Serious Injury or Death From Poisoning5 Jul 2025 · nafdac.gov.ngThe National Agency for Food and Drug Administration and Control (NAFDAC) is alerting the public about a recall of some batches of multivitamins and iron Supplements in the USA.These brands of vitamins, known as  CINCINNATI (WKRC), sold nationwide at retailers such as Walmart, Amazon, and Target, are being recalled due…Public Alert No. 0035/2022 – European Rapid Alert System For Dangerous Non-Food Products: Banned Cosmetic Product-Professional Mouse Pro-Vitamin B5 By United Kingdom Studio 2000 System21 Aug 2022 · nafdac.gov.ng, The National Agency for Food and Drug Administration and Control (NAFDAC)has received safety information from European Rapid Alert System for dangerous non- food products that a cosmetic product; Professional Mouse Pro-Vitamin B5 manufactured by United Kingdom Studio 2000 system has been banned. The product contains …Public Alert No. 0010/2021 – Falsified Vitamin A (Retinol) Identified In WHO Region of Africa7 Apr 2021 · nafdac.gov.ng, The National Agency for Food and Drugs Administration and Control (NAFDAC) has been notified by World Health Organization (WHO) on the circulation of two versions of falsified VITAMIN A (retinol) identified in Chad. Laboratory analysis of recovered samples revealed that both products are severely degraded and contain…Public Alert No. 0028/2018 – Recall Of Malco Vitamin B Complex Injection Manufactured By Shreechem Pharmaceuticals PVT. Limited13 Oct 2018 · nafdac.gov.ngThe National Agency for Food and Drug Administration and Control has been informed that the Zambia Medicines Regulatory Authority (ZARMA) has directed International Drug Company (IDC) Limited, Lusaka, Zambia to recall all batches of Malco (Vitamin B Complex) injection manufactured by Shreechem Pharmaceuticals PVT Limit…

Compare the brands and batch numbers in these notices with your pack, or enter your batch number above.

Check your pack of Vitamin E 400 IU Soft 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 Fuentes oficiales: FDA de EE. UU. · EMA (UE) · NAFDAC · alertas de la OMS

About Vitamin E 400 IU Soft Gel

What is in Vitamin E 400 IU Soft Gel?

Vitamin E 400 IU Soft Gel contains Tocopherol (vitamin E) (440 mg), as capsule, according to its NAFDAC registration record.

Is Vitamin E 400 IU Soft Gel registered with NAFDAC?

Yes. Vitamin E 400 IU Soft Gel is listed on the NAFDAC register under registration number A4-8322, and its registration is active as of 1 November 2026.

Has Vitamin E 400 IU Soft Gel been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Vitamin E 400 IU Soft Gel in our automatically synced alert list.

How can I check that my pack of Vitamin E 400 IU Soft Gel is genuine?

Run a free authenticity scan with the NAFDAC number A4-8322, 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 Vitamin E 400 IU Soft Gel?

Follow your prescription or the leaflet in your pack. The official label says: Before, during and/or after pregnancy, one softgel daily or as directed by a physician.…

What is Vitamin E 400 IU Soft Gel used for?

INDICATIONS: PNV-DHA is a multivitamin/multimineral fatty acid dietary supplement indicated for use in improving the nutritional status of women throughout pregnancy and in the postnatal period for both lactating and nonlactating mothers. (Summarised from the official U.S. FDA label for tocopherol (vitamin e). Always follow your doctor or pharmacist.)

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