XHC-075

XHC-075 is an FDA-registered drug product whose active ingredient is ALCOHOL. It is labelled by Ecolab Inc. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 47593-658, application 505G(a)(3), label effective 20260507. It is one of 582 FDA drug label records sharing the active ingredient 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.

Across FDA labelling, products containing ALCOHOL are most often described in connection with: hand washing, decrease bacteria. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses for hand washing to decrease bacteria on the skin

Directions wet hands thoroughly with product and allow to dry without wiping do not use if hands are visibly dirty or greasy; wash hands with soap and water instead

Warnings For external use only FLAMMABLE, keep away from fire or flame, heat, sparks and sources of static discharge. Do not use in eyes When using this product if in eyes, rinse promptly and throughly with water discontinue use if irritation and redness develop Stop use and ask doctor if skin irritation and redness persists from more than 72 hours Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

FDA lists 582 drug label records with 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 XHC-075 used for?
Uses for hand washing to decrease bacteria on the skin

Who makes XHC-075?
Ecolab Inc. is the labeler of record for XHC-075. 582 FDA label records share the active ingredient 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 XHC-075 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 XHC-075 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 ALCOHOL?
Yes. 582 FDA drug label records list 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 XHC-075 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.