Moxie

Moxie is an FDA-registered drug product whose active ingredient is ETHYL ALCOHOL. It is labelled by Apollo Health and Beauty Care taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 63148-660, application 505G(a)(3), label effective 20260505. 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: personal hand, hygiene help, spread bacteria, washing soap. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses For Personal hand hygiene to help the spread of bacteria. Can be used in place of hand washing if soap and water are not available.

Directions For occasional and personal use Rub thoroughly into hands for at least 30 seconds. Allow to dry Children under 6 years should be supervised when using this product

Warnings For External use only Flammable Keep away from source of heat or fire. When using this product Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water. Do not Inhale. Do not use on children less than 2 months of age on open skin wounds on broken or damaged skin Stop use and ask a doctor If Irritation or redness develops and lasts. Keep out of reach of children In case of accidental ingestion, get medical help or contact a Poison Control Centre immediately

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 Moxie used for?
Uses For Personal hand hygiene to help the spread of bacteria. Can be used in place of hand washing if soap and water are not available.

Who makes Moxie?
Apollo Health and Beauty Care is the labeler of record for Moxie. 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 Moxie 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 Moxie 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 Moxie 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.