Slf Hand Sanitizer — NAFDAC A3-100993: Is It Genuine? Uses, Alerts

Producto: Slf Hand Sanitizer
Número NAFDAC: A3-100993
Principio activo: Hand Sanitizer
Dosis: NA
Forma: NA
Tamaño del envase: 1 x 250 mL
Fabricante: No Constan
Solicitante (titular): Shulifang Biotechnology FZE
Approved: 5 Jul 2023
Estado: Activo Ver en NAFDAC ↗
Registro válido hasta: 5 Jul 2028
Alertas de la OMS: No se ha encontrado ninguno
Informes de la comunidad: Ninguno
Tiempos comprobados: 0

Pero sobre el medicamento, Hand sanitizer: uses, dosage and brands worldwide

Lo que encontramos

Slf Hand Sanitizer is on the NAFDAC register with an active registration (A3-100993). 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 Slf Hand Sanitizer

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

For hand washing to decrease bacteria on the skin.

Cómo tomarlo y con qué frecuencia

Dosage and Admistration Wet hands thoroughly with product and allow to dry without wiping.

Warnings

Warnings• For external use only • Flammable, keep away from fire or flame • Do not use in eyes. In case of contact, rinse eyes thorougly with water. • Discontinue use if irritation and redness develop.If condition persists for more than 72 hours consult a doctor.

How to store it

Keep out of reach of children.

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.

Recuérdame tomarlo Prospecto oficial completo

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 2024-11-07.

Label for hand sanitizer, the active ingredient registered with NAFDAC.

NAFDAC recall & alert notices

Public Alert No. 018/2025 – Alert on the Ban of Dove Hand and Deodorant Soap due to Butylphenyl Methylpropional (BMHCA) Contamination2 Jun 2025 · nafdac.gov.ngThe National Agency for Food and Drug Administration and Control (NAFDAC) is notifying the public that European Union Authorities have placed a ban on the marketing and sale of Dove Hand Soap (100g) and Dove Deodorant in Brussel, Belgium.The products do not comply with the Cosmetic Products Regulation as they are said …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.0046/2021 – American Screening LLC Issues A Voluntary Nationwide Recall Of American Screening Hand Sanitizer Packaged In 8 Oz Bottles Because They Resemble Beverage Containers7 Dec 2021 · nafdac.gov.ng, The National Agency for Food and Drug Administration and Control (NAFDAC) has been informed by U.S Food and Drug Administration (FDA) that American screening LLC issues a voluntary recall of American screening hand sanitizer packaged in 8 oz bottles because they resemble beverage containers. Risk Associated Ingesting…Public Alert No.0040/2021 – FDA Updates On Hand Sanitizers Consumers Should Not Use: Update – CDER Alert21 Oct 2021 · nafdac.gov.ng, The National Agency for Food and Drug Administration and Control (NAFDAC) has been informed by U.S Food and Drug Administration (FDA) about a safety communication that the agency has tested certain artnaturals scent free hand sanitizer labeled with “DIST. by artnaturals Gardena, CA 90248” and found unacceptable level…

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

Check your pack of Slf Hand Sanitizer

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

Te quedan 3 verificaciones gratis hoy Official sources: U.S. FDA · EMA (EU) · Health Canada · WHO alerts

About Slf Hand Sanitizer

What is in Slf Hand Sanitizer?

Slf Hand Sanitizer contains Hand Sanitizer (NA), as na, according to its NAFDAC registration record.

Is Slf Hand Sanitizer registered with NAFDAC?

Yes. Slf Hand Sanitizer is listed on the NAFDAC register under registration number A3-100993, and its registration is active as of 6 November 2026.

Has Slf Hand Sanitizer been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Slf Hand Sanitizer in our automatically synced alert list.

How can I check that my pack of Slf Hand Sanitizer is genuine?

Run a free authenticity scan with the NAFDAC number A3-100993, 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 Slf Hand Sanitizer?

Follow your prescription or the leaflet in your pack. The official label says: Dosage and Admistration Wet hands thoroughly with product and allow to dry without wiping.…

What is Slf Hand Sanitizer used for?

For hand washing to decrease bacteria on the skin. (Summarised from the official U.S. FDA label for hand sanitizer. 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.