Active Ingredient
Aluminum Zirconium Tetrachlorohydrex Gly 19% (anhydrous)
Brut Arctic Force
FDA Label NDC 41595-7015
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 Arctic Force (NDC 41595-7015). 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
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?
1-800-487-7273
©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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