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Slf Hand Sanitizer

NAFDAC REG NO: A3-100993 Médicament

Enregistré auprès de NAFDAC. Enregistrement actifAs of 30 October 2026 · synced automatically from official sources.
Produit
Slf Hand Sanitizer
Numéro NAFDAC
A3-100993
Principe actif
Hand Sanitizer
Dosage
N/A
Forme
N/A
Conditionnement
1 x 250 mL
Fabricant
Non répertorié
Déposant / Titulaire :
Shulifang Biotechnology FZE
Approuvé
5 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: Hand sanitizer: uses, dosage and brands worldwide

What we found

  • 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.

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 Slf Hand Sanitizer

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

(s) For handwashing to decrease bacteria on the skin

Comment le prendre et à quelle fréquence

Wet hands thoroughly with product and allow to dry without wiping

While you are taking it

• Avoid contact with eyes • In case of eye contact, rinse with water to remove

Talk to a doctor first if

In the eyes

Warnings

For External Use Only Flammable. Keep away from fire or flame Do not use In the eyes When using this product • Avoid contact with eyes • In case of eye contact, rinse with water to remove Stop use and ask a doctor if Irritation and redness develop Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Effets secondaires possibles

Irritation and redness develop

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 2025-12-15.

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.

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Encore 3 vérifications gratuites aujourd'hui Sources officielles : FDA américaine · EMA (UE) · NAFDAC · alertes OMS

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 30 October 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: Wet hands thoroughly with product and allow to dry without wiping…

What is Slf Hand Sanitizer used for?

(s) For handwashing 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.