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Biu-Care Infusion Given Set

NAFDAC Reg. No. A3-100869 · Drug

Registered with NAFDAC — registration activeAs of 5 November 2026 · synced automatically from official sources.
Product
Biu-Care Infusion Given Set
NAFDAC number
A3-100869
Active ingredient
Infusion Set
Strength
NA
Form
NA
Pack size
50 pieces per pack
Manufacturer
Not listed
Applicant (holder)
Biurette Nig. Ltd
Approved
27 Jan 2023
Status
Active View on NAFDAC ↗
Registration valid to
25 Jan 2028
WHO alerts
None found
Community reports
None
Times checked
0

RxVerify commentary

  • Biu-Care Infusion Given Set is on the NAFDAC register with an active registration (A3-100869). 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 Biu-Care Infusion Given Set is used for

From the official U.S. FDA label for infusion set, the active ingredient registered with NAFDAC.

What it is used for

Temporarily protects and helps relieve dry or cracked skin Beneficlal for face, hands, body, and legs

Purpose

After cleansing andtoning, take an appropriate amount ofthis product and apply it evenly on theface, massage until absorbed

Warnings

Risk InformationFor external use only Mention de risquesPour usage externe seulement Do not use on damaged or broken skin. Ne pas utiliser sur la peau endommagée ou avec des lésions If rash occurs, discontinue use and consult a health care practitioner. En présence d'une éruption cutanée, cesser l'utilisation et consulter un praticien de soins de santé When using this product keep out of eyes. Rinse with water to remove. Eviter tout contact avec les yeux. Rincer a l'eau le cas échéant Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. …

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

NAFDAC recall & alert notices

Public Alert No. 033/2024 – Alert on the Recall of Radox Care + Moisturise Liquid Hand Wash due to presence of Butyphenyl Methylpropional (BMHCA) Content22 Aug 2024 · nafdac.gov.ngThe National Agency for Food and Drugs Administration and Control (NAFDAC) is notifying the public of the recall of Radox Care + Moisturise Liquid Hand Wash by the European Union (EU) in Brussels, Belgium.The product does not comply with the Cosmetic Products Regulation as it is said to contain Butyphenyl Methylpropion…Public Alert No.022/2021 – Update: FDA Recommends Transition from Use of Non-NIOSH-Approved and Decontaminated Disposable Respirators – Letter to Health Care Personnel and Facilities8 Jul 2021 · nafdac.gov.ng, The National Agency for Food and Drug Administration and Control (NAFDAC) has been informed that the U.S. Food and Drug Administration (FDA) is recommending health care personnel and facilities to transition away from crisis capacity conservation strategies, such as using non-NIOSH-approved disposable respirators, in…Important Covid-19 Vaccine Safety Communication To Healthcare Providers27 May 2021 · nafdac.gov.ng, Important Covid-19 Vaccine Safety Communication To Healthcare Providers KEY POINTS    Possible Rare Event, Severe Allergic Reactions (Anaphylaxis) and Thromboembolic Events with Some Covid-19 Vaccines (probably due to underlying medical conditions and use of certain medications). Possible contraindications with Non…Public Alert No: 39/2020 – Alert on Happy Ducts Compress, Cord Care and Goldenseal Powder by WishGarden Herbs Due to Bacterial Contamination30 Dec 2020 · nafdac.gov.ng, The National Agency for Food and Drug Administration and Control (NAFDAC) has received information from the US FDA about voluntary recall of some lots of Happy Ducts Compress, Cord Care and Goldenseal Powder by WishGarden Herbs. The recall is due to a possible supply chain contamination with the bacteria Cronobacter …

Notices list affected brands and batch numbers — compare them with your pack. Enter your batch number above to check it automatically.

Check your pack of Biu-Care Infusion Given Set

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 Biu-Care Infusion Given Set

What is in Biu-Care Infusion Given Set?

Biu-Care Infusion Given Set contains Infusion Set (NA), as na, according to its NAFDAC registration record.

Is Biu-Care Infusion Given Set registered with NAFDAC?

Yes. Biu-Care Infusion Given Set is listed on the NAFDAC register under registration number A3-100869, and its registration is active as of 5 November 2026.

Has Biu-Care Infusion Given Set been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Biu-Care Infusion Given Set in our automatically synced alert list.

How can I check that my pack of Biu-Care Infusion Given Set is genuine?

Run a free authenticity scan with the NAFDAC number A3-100869, 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 Biu-Care Infusion Given Set used for?

Temporarily protects and helps relieve dry or cracked skin Beneficlal for face, hands, body, and legs (Summarised from the official U.S. FDA label for infusion set. 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.