Überprüfung…
Automatisch übersetzt. Dosierung und Warnhinweise: bitte im englischen Original prüfen. Auf Englisch lesen
Homepage / Arzneimittel A–Z / Disinfectant

Disinfectant

[s] Sanitizing wipe to help reduce bacteria that potentially can cause disease.

Sold without prescription in some countries Topical Safety alerts on record

How to use Disinfectant

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

Who it is for

[s] Sanitizing wipe to help reduce bacteria that potentially can cause disease.

How to take it and how often
  • Wipe hands or all surfaces
  • Allow to dry
  • Supervise
  • Children under 6 years of age when using this product to avoid swallowing
While you are taking it
  • Keep out of eyes, ears, and mouth
  • In case of contact with eyes, rinse eyes thoroughly with water
Talk to a doctor first if

in children less than 2 months of age. on open skin wounds Do not re-use wipes

Warnings

For external use only. Flammable. Keep away from heat or flame Do not use in children less than 2 months of age. on open skin wounds Do not re-use wipes When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water. Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away.

How to store it

Keep out of reach of children.

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 2026-02-03.

Brands around the world

Products with Disinfectant as the active ingredient. Names differ between countries.

Registered products

United States (FDA)

75% Alcohol DisinfectantALCOHOL 75 mL/100mL · Liquid · Zhejiang Meimi Technology Co., Ltd.
NDC 41366-015Label
75% Alcohol DisinfectantALCOHOL 75 mL/100mL · Liquid · Zhejiang Meimi Technology Co., Ltd.
NDC 41366-016Label
Latalia Alcohol Disinfectant WipesALCOHOL 80 mL/100mL · Cloth · INTERNATIONAL CONSUMER PRODUCTS (PVT.) LTD
NDC 80016-006Label

Nigeria (NAFDAC)

NAFDACTCH Hypochlorous A3-101273NAFDACVincal Water Sure A3-101163NAFDACUcan Public Places A3-100664NAFDACWater Guard Plus Powder 03-3341NAFDACMorigad Lysol Disinfectant 04-0962NAFDACAqua Salveo Water Disinfectant A3-100442NAFDACZymokleen Disinfectant Cleaner A3-100596NAFDACCorysan Antiseptic Disinfectant A11-0324NAFDACAnosan Eco (Room Hygiene & Nebulization) A3-100834NAFDACAnosan Aqua (Drinking Water Disinfection) A3-100915NAFDACTetmosol Protect Plus Antiseptic Disinfectant A11-0143NAFDACAnosan (Naturlicch Rein Surface Disinfection) A3-100836

Other countries: check your pack's registration number and we point you to your regulator.

Safety alerts and recalls

Wyandotte, Sanifect E3, Hand Sanitizer (Ethanol-Based, Product 5511), Ethyl Alcohol 60.1%, Manufacture By: AFCO, 550 Development Avenue, Chambersburg, PA 17210, Toll Free: 800-345-U.S. FDA Class II
29 Sep 2025 · Acuity Specialty Products, Inc. · OngoingcGMP deviations: The recall was initiated because required receipt testing of incoming alcohol components used to manufacture the listed hand sanitizers was not performed, so methanol risk could not be excluded.
Spectrum Advanced Gel Hand Sanitizer, Ethyl alcohol 70%, 8 FL OZ (236 mL) per bottle, Manufactured for Medline Industries, Inc., Three Lakes Drive, Northfield, IL 60693 USA. NDC: U.S. FDA Class II
23 May 2025 · Consumer Product Partners, LLC · OngoingSubpotent product: Product has cloudy appearance and tested below assay label claim for 70% Ethyl Alcohol
OralProCare medicated lip treatment, Net Wt 9.9 g (0.35 oz) tube, Ethyl alcohol 6.0% Antibacterial, Manufactured by: Den-Mat Holdings, LLC, Lompoc, CA, 93436, USA, NDC 59883-500-01U.S. FDA Class II
16 Jan 2024 · Den-Mat Holdings, LLC · OngoingCGMP Deviations: products may not conform to the labeled specifications.
Equate Hand Sanitizer (Ethyl Alcohol 62%), 7.5 FL.OZ. (221 mL) UPC 6 81131 05961 9U.S. FDA Class II
20 Oct 2023 · Omega & Delta Co., Inc. · OngoingSub Potent and Super Potent Product: During an impact assessment of the DOP Hand Sanitizer product, it was identified that several lots distributed did not comply with the finished good acceptance criteria established.

A recall usually affects certain batches only. Compare the lot number on your pack.

Check your pack of Disinfectant

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

Questions about Disinfectant

What is Disinfectant used for?

[s] Sanitizing wipe to help reduce bacteria that potentially can cause disease. (From the official U.S. FDA label.)

How do I take Disinfectant?

Follow your prescription or the leaflet in your pack. The official label says: Wipe hands or all surfaces. Allow to dry. Supervise children under 6 years of age when using this product to avoid swallowing.…

Do I need a prescription for Disinfectant?

In many countries Disinfectant is sold without a prescription in some strengths. Rules differ by country, so ask a pharmacist.

What brands contain Disinfectant?

Disinfectant is sold under names such as Latalia Alcohol Disinfectant Wipes. Brand names differ between countries.

How can I check that my Disinfectant is genuine?

Scan the registration number on your pack with PillVera (NAFDAC number in Nigeria, NDC in the United States, DIN in Canada), check the expiry date and buy only from licensed pharmacies.