VANILLA HYDRATING HAND SANITIZER

VANILLA HYDRATING HAND SANITIZER is an FDA-registered drug product whose active ingredient is ALCOHOL ANTISEPTIC. It is labelled by Kingkey MBC Life Technology Group Co.,Ltd taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 73928-535, application M003, label effective 20260626. It is one of 54 FDA drug label records sharing the active ingredient ALCOHOL ANTISEPTIC. 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 ANTISEPTIC are most often described in connection with: users hand, sanitizer help, reduce bacteria, cause disease. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Users Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings Flammable. Keep away from fire or flame. For external use only. Do not use it near eye area. In case of contact, rinse eyes thoroughly with water. Stop use and ask a doctor if irritation or rash appears and lasts. Keep out of reach of children. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

FDA lists 54 drug label records with ALCOHOL ANTISEPTIC 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 VANILLA HYDRATING HAND SANITIZER used for?
Users Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Who makes VANILLA HYDRATING HAND SANITIZER?
Kingkey MBC Life Technology Group Co.,Ltd is the labeler of record for VANILLA HYDRATING HAND SANITIZER. 54 FDA label records share the active ingredient ALCOHOL ANTISEPTIC, 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 VANILLA HYDRATING HAND SANITIZER 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 VANILLA HYDRATING HAND SANITIZER 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 ANTISEPTIC?
Yes. 54 FDA drug label records list ALCOHOL ANTISEPTIC 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 VANILLA HYDRATING HAND SANITIZER 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.