Harris Teeter

Harris Teeter is an FDA-registered drug product whose active ingredient is ISOPROPYL ALCOHOL. It is labelled by Harris Teeter, LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 69256-970, application M003, label effective 20260902. It is one of 128 FDA drug label records sharing the active ingredient ISOPROPYL 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 ISOPROPYL ALCOHOL are most often described in connection with: first aid, help prevent, risk infection, minor cuts. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses first aid to help prevent the risk of infection in minor cuts, scrapes and burns

Directions clean the affected area discard after a single use may be covered with a sterile bandage

Warnings For external use only. Flammable, keep away from fire or flame. When using this product do not get in the eyes or apply over large areas of the body in case of deep or puncture wounds, animal bites or serious burns, consult a doctor do not use longer than 1 week unless directed by a doctor Stop use and ask a doctor if the condition persists or gets worse Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

FDA lists 128 drug label records with ISOPROPYL 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.

5 FDA recall record(s) match this product name or manufacturer. A match means the firm or product name appears in the enforcement report; confirm lot numbers and dates against the official FDA notice before acting.

What is Harris Teeter used for?
Uses first aid to help prevent the risk of infection in minor cuts, scrapes and burns

Who makes Harris Teeter?
Harris Teeter, LLC is the labeler of record for Harris Teeter. 128 FDA label records share the active ingredient ISOPROPYL 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 Harris Teeter 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 Harris Teeter 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 ISOPROPYL ALCOHOL?
Yes. 128 FDA drug label records list ISOPROPYL 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 Harris Teeter been recalled?
5 FDA recall record(s) match this product name or manufacturer. Review the recall and safety notices section on this page and confirm lot numbers against the official FDA enforcement report.

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.