ZERMMAT-ALEXIS ANTIPERSPIRANT DEODORANT ROLL-ON FOR MEN

ANTIPERSPIRANT DEODORANT ROLL-ON CUTANEOUS HUMAN OTC DRUG

ZERMMAT-ALEXIS ANTIPERSPIRANT DEODORANT ROLL-ON FOR MEN is an FDA drug label for the active ingredient ANTIPERSPIRANT DEODORANT ROLL-ON manufactured by EVI LABS administered by CUTANEOUS. 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 20260427.

Generic name
ANTIPERSPIRANT DEODORANT ROLL-ON
Manufacturer
EVI LABS
Product type
HUMAN OTC DRUG
Route
CUTANEOUS
Dosage form
N/A
NDC
84178-021
Application
M019
Label effective
20260427

About this product

ZERMMAT-ALEXIS ANTIPERSPIRANT DEODORANT ROLL-ON FOR MEN is an FDA-registered drug product whose active ingredient is ANTIPERSPIRANT DEODORANT ROLL-ON. It is labelled by EVI LABS taken by cutaneous and marketed as a human otc drug product. Identifiers on file: NDC 84178-021, application M019, label effective 20260427. It is one of 12 FDA drug label records sharing the active ingredient ANTIPERSPIRANT DEODORANT ROLL-ON. 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 ANTIPERSPIRANT DEODORANT ROLL-ON are most often described in connection with: reduces underarm. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active Ingredients Aluminum Chlorohydrate 10 %

Indications & Usage

Uses Reduces underarm perspiration

Dosage & Administration

Directions Shake well before use. Apply to the underarms only. Close tightly after use

Warnings

Warning For external use only.

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How products containing ANTIPERSPIRANT DEODORANT ROLL-ON compare

FDA lists 12 drug label records with ANTIPERSPIRANT DEODORANT ROLL-ON 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
— — EVI LABS 10
— — EVI LALBS 2
— — — —
— — — —
— — — —

Frequently asked questions

What is ZERMMAT-ALEXIS ANTIPERSPIRANT DEODORANT ROLL-ON FOR MEN used for?
Uses Reduces underarm perspiration

Who makes ZERMMAT-ALEXIS ANTIPERSPIRANT DEODORANT ROLL-ON FOR MEN?
EVI LABS is the labeler of record for ZERMMAT-ALEXIS ANTIPERSPIRANT DEODORANT ROLL-ON FOR MEN. 12 FDA label records share the active ingredient ANTIPERSPIRANT DEODORANT ROLL-ON, 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 ZERMMAT-ALEXIS ANTIPERSPIRANT DEODORANT ROLL-ON FOR MEN come in?
administered by cutaneous. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is ZERMMAT-ALEXIS ANTIPERSPIRANT DEODORANT ROLL-ON FOR MEN 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 ANTIPERSPIRANT DEODORANT ROLL-ON?
Yes. 12 FDA drug label records list ANTIPERSPIRANT DEODORANT ROLL-ON 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 ZERMMAT-ALEXIS ANTIPERSPIRANT DEODORANT ROLL-ON FOR MEN 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.