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Vitamin E 400 IU Soft Gel

NAFDAC Reg. No. A4-8322 · Drug

Registered with NAFDAC. Registration activeAs of 1 November 2026 · synced automatically from official sources.
Product
Vitamin E 400 IU Soft Gel
NAFDAC number
A4-8322
Active ingredient
Tocopherol (vitamin E)
Strength
440 mg
Form
Capsule
Pack size
3 x 10's (in PVC blisters)
Manufacturer
Not listed
Applicant (holder)
Emzor Pharmaceutical Industries Limited
Approved
31 Oct 2023
Status
Active View on NAFDAC ↗
Registration valid to
30 Oct 2028
WHO alerts
None found
Community reports
None
Times checked
0

About the medicine: Tocopherol: uses, dosage and brands worldwide

What we found

  • 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.

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 Vitamin E 400 IU Soft Gel

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

Serious warning: 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. …
Who it is 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.

How to take it and how often

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.

Possible side effects

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

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 2026-07-23.

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.

Or take photos of the pack
3 free checks left today Official sources: U.S. FDA · EMA (EU) · NAFDAC · WHO alerts

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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