Lume Deodorant with Clinical Strength Sweat Control Soft Powder

Lume Deodorant with Clinical Strength Sweat Control Soft Powder is an FDA-registered drug product whose active ingredient is ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY. It is labelled by Lume Deodorant, LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 84520-036, application M019, label effective 20260708. It is one of 21 FDA drug label records sharing the active ingredient ALUMINUM ZIRCONIUM TRICHLOROHYDREX 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 TRICHLOROHYDREX GLY are most often described in connection with: reduces underarm, wetness extra. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Reduces underarm wetness extra effective

Apply to underamrs Apply to dry skin Apply at bedtime

For external use only

FDA lists 21 drug label records with ALUMINUM ZIRCONIUM TRICHLOROHYDREX 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 Lume Deodorant with Clinical Strength Sweat Control Soft Powder used for?
Reduces underarm wetness extra effective

Who makes Lume Deodorant with Clinical Strength Sweat Control Soft Powder?
Lume Deodorant, LLC is the labeler of record for Lume Deodorant with Clinical Strength Sweat Control Soft Powder. 21 FDA label records share the active ingredient ALUMINUM ZIRCONIUM TRICHLOROHYDREX 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 Lume Deodorant with Clinical Strength Sweat Control Soft Powder 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 Lume Deodorant with Clinical Strength Sweat Control Soft Powder 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 TRICHLOROHYDREX GLY?
Yes. 21 FDA drug label records list ALUMINUM ZIRCONIUM TRICHLOROHYDREX 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 Lume Deodorant with Clinical Strength Sweat Control Soft Powder 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.