MG DermaSpray 70

MG DermaSpray 70 is an FDA-registered drug product whose active ingredient is ETHYL ALCOHOL. It is labelled by Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 50241-486, application M, label effective 20260804. 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.

Across FDA labelling, products containing ETHYL ALCOHOL are most often described in connection with: directions wash, water rinse, wet entire, surface hands, product especially, fingernails rub, together until, re-apply needed. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Directions Wash hands with soap and water. Rinse with potable water. Wet entire surface of hands with product, especially the cuticles and fingernails. Rub hands together until dry. Do not Rinse hands. Re-apply as needed.

Uses For hand sanitizing to decrease bacteria on the skin

Warnings For external use only. Flammable keep away from fire or flame

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 MG DermaSpray 70 used for?
Directions Wash hands with soap and water. Rinse with potable water. Wet entire surface of hands with product, especially the cuticles and fingernails. Rub hands together until dry. Do not Rinse hands. Re-apply as needed.

Who makes MG DermaSpray 70?
Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc. is the labeler of record for MG DermaSpray 70. 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 MG DermaSpray 70 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 MG DermaSpray 70 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 MG DermaSpray 70 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.