FDA.reportPublic FDA data

Brut Arctic Force

Manufacturer
Idelle Labs, Ltd | Les Emballages Knowlton, Inc.
Effective date
2018-04-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:55:10

Label at a glance#

ProductBrut Arctic Force
Active ingredientALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
Label structure13 sections

Dosage and administration

Apply to underarms only

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

BRUT® ARCTIC FORCE™

48H UNBEATABLE ODOR & WETNESS PROTECTION

ANTIPERSPIRANT+DEODORANT

Net Wt 2 oz (56 g)

LONG LASTING WETNESS & ODOR PROTECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Zirconium Tetrachlorohydrex Gly 19% (anhydrous)

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Use

INDICATIONS & USAGE SECTION

Reduces underarm wetness

Warnings

WARNINGS SECTION

For external use only.

Stop use if

OTC - STOP USE SECTION

Rash or irritation occurs.

Do not use

OTC - DO NOT USE SECTION

On broken skin.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

Kidney disease.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply to underarms only

Inactive ingredients

INACTIVE INGREDIENT SECTION

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?

OTC - QUESTIONS SECTION

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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description
image description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
41595-7015-12020-01-31C16284748780-19d75b9d1-0102-f424-e053-dadaa90a57ceBRUT ® ARCTIC FORCE ™

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
41595-7015-1Brut Arctic Force56 g in 1 CANISTERSTICK561

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
41595-7015BRUT ARCTIC FORCE (ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY) STICK [IDELLE LABS, LTD]1Legacy NDC, 1 package rows20180405_c9296f0e-14ce-4cac-bb17-aedf9a8cce4a.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
41595-701541595-7015-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY8O386558JEACTIB
CYCLOMETHICONE 50THT5PCI0RIACT
STEARYL ALCOHOL2KR89I4H1YIACT
PPG-14 BUTYL ETHERR199TJT95TIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
TALC7SEV7J4R1UIACT
PEG-8 DISTEARATE7JNC8VN07MIACT
CANOLA OIL331KBJ17RKIACT
CORN OIL8470G57WFMIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
TERT-BUTYLHYDROQUINONEC12674942BIACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
dcd6d7c7-29b7-450d-9191-1f0d2ff225ecc9296f0e-14ce-4cac-bb17-aedf9a8cce4a2018-04-05WarningsExact identifier
spl id: dcd6d7c7-29b7-450d-9191-1f0d2ff225ec
spl set id: c9296f0e-14ce-4cac-bb17-aedf9a8cce4a

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.