Lightning X Hand Cleanser

Lightning X Hand Cleanser is an FDA-registered drug product whose active ingredient is ETHYL ALCOHOL. It is labelled by Nantong Health & Beyond Hygienic Products Inc. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 43473-122, application M005, label effective 20260511. It is one of 184 FDA drug label records sharing the active ingredient ETHYL ALCOHOL. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

indication

dosage

warning

FDA lists 184 drug label records with ETHYL ALCOHOL as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

What is Lightning X Hand Cleanser used for?
indication

Who makes Lightning X Hand Cleanser?
Nantong Health & Beyond Hygienic Products Inc. is the labeler of record for Lightning X Hand Cleanser. 184 FDA label records share the active ingredient ETHYL ALCOHOL, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does Lightning X Hand Cleanser come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is Lightning X Hand Cleanser prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Are there other products containing ETHYL ALCOHOL?
Yes. 184 FDA drug label records list ETHYL ALCOHOL as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has Lightning X Hand Cleanser been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.