Mando Deodorant Extra Strength Sweat Control Pro Sport

ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY TOPICAL HUMAN OTC DRUG

Mando Deodorant Extra Strength Sweat Control Pro Sport is an FDA drug label for the active ingredient ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY manufactured by Lume Deodorant, LLC administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260616.

Generic name
ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY
Manufacturer
Lume Deodorant, LLC
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
84520-030
Application
M019
Label effective
20260616

About this product

Mando Deodorant Extra Strength Sweat Control Pro Sport 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 84520-030, application M019, label effective 20260616. 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.

What it is used for

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.

Active ingredients

Active Ingredient Aluminum Zirconium Trichlorohydrex Gly 20%

Indications & Usage

reduces underarm wetness extra effective

Dosage & Administration

apply to underarms only apply to dry skin apply at bedtime

Warnings

For external use only

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ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY

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Lume Deodorant with Clinical Strength Sweat Control Vanilla Bliss

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How products containing ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY compare

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.

Dosage formProductsManufacturerProducts
— — The Procter & Gamble Manufacturing Company 9
— — Lume Deodorant, LLC 6
— — Bath and Body Works, Distr. 3
— — Harry's Inc. 1
— — Harry's, Inc. 1

Frequently asked questions

What is Mando Deodorant Extra Strength Sweat Control Pro Sport used for?
reduces underarm wetness extra effective

Who makes Mando Deodorant Extra Strength Sweat Control Pro Sport?
Lume Deodorant, LLC is the labeler of record for Mando Deodorant Extra Strength Sweat Control Pro Sport. 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 Mando Deodorant Extra Strength Sweat Control Pro Sport 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 Mando Deodorant Extra Strength Sweat Control Pro Sport 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 Mando Deodorant Extra Strength Sweat Control Pro Sport 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.

This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.