Humco Iodides Tincture

Humco Iodides Tincture is an FDA-registered drug product whose active ingredient is ETHYL ALCOHOL. It is labelled by Humco Holding Group, Inc. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 0395-1207, application M003, label effective 20231215. 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: first aid, help prevent, infection minor, cuts scrapes. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses First aid to help prevent infection in minor cuts, scrapes and burns.

Directions Clean the affected area. Aply a small amount to the affected area 1 to 3 times daily. May be covered with a sterile bandage. If bandaged, let it dry first.

Warnings For external use only.

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 Humco Iodides Tincture used for?
Uses First aid to help prevent infection in minor cuts, scrapes and burns.

Who makes Humco Iodides Tincture?
Humco Holding Group, Inc. is the labeler of record for Humco Iodides Tincture. 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 Humco Iodides Tincture 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 Humco Iodides Tincture 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 Humco Iodides Tincture 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.