BRUT SIGNATURE ANTI-PERSPIRANT AND DEODORANT- aluminum zirconium trichlorohydrex gly stick

Brut Signature Anti-Perspirant and Deodorant by

Drug Labeling and Warnings

Brut Signature Anti-Perspirant and Deodorant by is a Otc medication manufactured, distributed, or labeled by Sodalis USA LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Aluminum Zirconium Trichlorohydrex Gly 16% (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, Dimethicone, Petrolatum, Hydrogenated Castor Oil, Talc, Fragrance, Mineral Oil, Behenyl Alcohol

Questions?

1-800-575-7960

Label 81277-001-01

Label 81277-001-02

INGREDIENTS AND APPEARANCE

BRUT SIGNATURE ANTI-PERSPIRANT AND DEODORANT 
aluminum zirconium trichlorohydrex gly stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81277-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY (UNII: T27D6T99LH) (ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY - UNII:T27D6T99LH)	ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY	19 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
PPG-14 BUTYL ETHER (UNII: R199TJT95T)
DIMETHICONE (UNII: 92RU3N3Y1O)
PETROLATUM (UNII: 4T6H12BN9U)
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
TALC (UNII: 7SEV7J4R1U)
MINERAL OIL (UNII: T5L8T28FGP)
DOCOSANOL (UNII: 9G1OE216XY)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81277-001-01	56 g in 1 CONTAINER; Type 0: Not a Combination Product	01/01/2010
2	NDC: 81277-001-02	76 g in 1 CONTAINER; Type 0: Not a Combination Product	01/01/2010

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M019	01/01/2010

Labeler - Sodalis USA LLC (119375257)