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Accueil / Enregistré au Nigeria / Azmu Auto Disable Syringe

Azmu Auto Disable Syringe

NAFDAC REG NO: A3-100997 Médicament

Enregistré auprès de NAFDAC. Enregistrement actifAs of 5 November 2026 · synced automatically from official sources.
Produit
Azmu Auto Disable Syringe
Numéro NAFDAC
A3-100997
Principe actif
Syringes
Dosage
N/A
Forme
N/A
Conditionnement
0.5 mL x 100; 0.05 mL x 100 pieces per pack
Fabricant
Non répertorié
Déposant / Titulaire :
Azmu Pharmaceuticals Limited
Approuvé
9 Jul 2023
Statut
Actif Vue sur NAFDAC ↗
Enregistrement valable jusqu'au
5 Jul 2028
Alertes OMS
Non trouvé
Community reports
None
Times checked
0

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

What we found

  • Azmu Auto Disable Syringe is on the NAFDAC register with an active registration (A3-100997). 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 Azmu Auto Disable Syringe

Ce que dit la notice officielle. Si un médecin vous l'a prescrit, suivez l'ordonnance. La notice de votre boîte prime si elle est différente.

Pour qui

• for hand sanitizing to decrease bacteria on skin when water and soap are not avaliable • recommended for repeated use

Comment le prendre et à quelle fréquence

• remove and unfold wipe •wet hands thoroughly with product and let air dry

Warnings

For external use only. Flammable keep away from fire or flame. When using this product do not use in or near eyes, if contact occurs, flush thoroughly with water. Stop use and contact a doctor if irritation or redness persists for more than 72 hours.

How to store it

Keep out of reach of children.

En cas d'oubli

Prenez-le dès que vous y pensez, sauf s'il est presque l'heure de la dose suivante. Dans ce cas, sautez la dose oubliée. Ne prenez jamais deux doses à la fois pour compenser. Vérifiez votre notice, certains médicaments font exception.

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 2025-09-30.

Label for Azmu Auto Disable Syringe, the active ingredient registered with NAFDAC.

Check your pack of Azmu Auto Disable Syringe

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

Ou prenez la boîte en photo
Encore 3 vérifications gratuites aujourd'hui Official sources: U.S. FDA · EMA (EU) · Health Canada · WHO alerts

About Azmu Auto Disable Syringe

What is in Azmu Auto Disable Syringe?

Azmu Auto Disable Syringe contains Syringes (NA), as na, according to its NAFDAC registration record.

Is Azmu Auto Disable Syringe registered with NAFDAC?

Yes. Azmu Auto Disable Syringe is listed on the NAFDAC register under registration number A3-100997, and its registration is active as of 5 November 2026.

Has Azmu Auto Disable Syringe been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Azmu Auto Disable Syringe in our automatically synced alert list.

How can I check that my pack of Azmu Auto Disable Syringe is genuine?

Run a free authenticity scan with the NAFDAC number A3-100997, 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 Azmu Auto Disable Syringe?

Follow your prescription or the leaflet in your pack. The official label says: • remove and unfold wipe •wet hands thoroughly with product and let air dry…

What is Azmu Auto Disable Syringe used for?

• for hand sanitizing to decrease bacteria on skin when water and soap are not avaliable • recommended for repeated use (Summarised from the official U.S. FDA label for Azmu Auto Disable Syringe. 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.