BRUT CLASSIC ANTIPERSPIRANT AND DEODORANT- aluminum chlorohydrate aerosol, spray

Brut Classic Antiperspirant and Deodorant by

Drug Labeling and Warnings

Brut Classic Antiperspirant 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 Chlorohydrate 20.9%

Purpose

Antiperspirant

Use

reduces underarm wetness

Warnings

For external use only.

• Flammable.Do not use when smoking or near fire, flame or heat.
• Contents under pressure
• Do not puncture or incinerate
• Do not store at temperature above 120ºF

Do not use

on broken skin

Ask a doctor before use if you have

kidney disease

When using this product

• Keep away from face and mouth to avoid breathing it
• Avoid spraying in eyes
• Use only as directed; intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal

Stop use if

rash or irritation occurs

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Shake well. Hold can 6 inches away from underarm and spray. Apply to underarms only.

Inactive ingredients:

Butane, Hydrofluorocarbon 152a, Cyclopentasiloxane, Aluminum Chlorohydrate, Isopropyl Palmitate, Talc, Disteardimonium Hectorite, Propylene Carbonate, Fragrance (Parfum), Amyl Cinnamal, Hydroxycitronellal, Coumarin, Linalool, Citronellol, alpha-hexylcinnaldehyde, d-Limonene, Hydroxyisohexyl 3-Cyclohexene, Carboxaldehyde.

Questions?

1-800-575-7960

Package Labelling:

INGREDIENTS AND APPEARANCE

BRUT CLASSIC ANTIPERSPIRANT AND DEODORANT 
aluminum chlorohydrate aerosol, spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81277-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M)	ALUMINUM CHLOROHYDRATE	20.9 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
BUTANE (UNII: 6LV4FOR43R)
1,1-DIFLUOROETHANE (UNII: 0B1U8K2ME0)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
TALC (UNII: 7SEV7J4R1U)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
.ALPHA.-AMYLCINNAMALDEHYDE (UNII: WC51CA3418)
HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)
COUMARIN (UNII: A4VZ22K1WT)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
.BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
.ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
HYDROXYISOHEXYL 3-CYCLOHEXENE CARBOXALDEHYDE (UNII: QUE43B9Z2Q)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81277-003-01	170 g in 1 CAN; Type 0: Not a Combination Product	01/25/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M019	01/25/2021

Labeler - Sodalis USA LLC (119375257)