Hand Antiperspirant Daily Use

Hand Antiperspirant Daily Use is an FDA-registered drug product whose active ingredient is ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY. It is labelled by Clutch Inc taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 74307-007, application M019, label effective 20260820. It is one of 22 FDA drug label records sharing the active ingredient ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY. 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 ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY are most often described in connection with: rash irritation. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Stop use if rash or irritation occurs

Directions wash and dry hands thoroughly before application Apply a single pump of product to palms each morning Rub Balms together vigorously for 30 seconds

Warnings For external use only. Do not use on broken or irritated skin Ask a doctor before use if you have kidney disease.

FDA lists 22 drug label records with ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY 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 Hand Antiperspirant Daily Use used for?
Stop use if rash or irritation occurs

Who makes Hand Antiperspirant Daily Use?
Clutch Inc is the labeler of record for Hand Antiperspirant Daily Use. 22 FDA label records share the active ingredient ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY, 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 Hand Antiperspirant Daily Use 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 Hand Antiperspirant Daily Use 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 ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY?
Yes. 22 FDA drug label records list ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY 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 Hand Antiperspirant Daily Use 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.