Brut
FDA Label NDC 41595-7013

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Idelle Labs, Ltd for the product Brut (NDC 41595-7013). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredient, purpose, use, warnings, stop use if, do not use, keep out of reach of children., ask a doctor before use if you have, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Aluminum Zirconium Tetrachlorohydrex Gly 19% (anhydrous)

Purpose

Antiperspirant

Use

Reduces underarm wetness

Warnings

For external use only.

Stop Use If

Rash or irritation occurs.

Do Not Use

On broken skin.

Keep Out Of Reach Of Children.

In case of ingestion, get medical help or contact a Poison Control Center right away.

Ask A Doctor Before Use If You Have

Kidney disease.

Directions

Apply to underarms only

Inactive Ingredients

Cyclopentasiloxane, Stearyl Alcohol, PPG-14 Butyl Ether, Hydrogenated Castor Oil, Talc, PEG-8 Distearate, Fragrance, Canola Oil Glyceride, Zea Mays (Corn) Oil, Propylene Glycol, Citric Acid, TBHQ, BHT

Questions?

Call 1-800-487-7273  

www.brutworld.com

©IDELLE LABS, LTD.

 All rights reserved.
 Made in CANADA.
 Distributed by Idelle Labs, Ltd., El Paso, TX 79912 USA.

Brut® is a trademark of Kaz Europe Sarl.

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