AXE- apollo dry spray antiperspirant 48hr protection dry aerosol, spray

Axe by

Drug Labeling and Warnings

Axe by is a Otc medication manufactured, distributed, or labeled by Conopco Inc. d/b/a/ Unilever. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

AXE APOLLO DRY SPRAY ANTIPERSPIRANT 48HR PROTECTION DRY - aluminum chlorohydrate aerosol, spray

Axe Apollo Dry Spray Antiperspirant 48HR Protection Dry

Drug Facts

Active ingredient
Aluminum Chlorohydrate (23.3%)

Purpose

antiperspirant

Uses

reduces underarm wetness

Warnings

For external use only
FLAMMABLE. DO NOT USE NEAR HEAT, FLAME, OR WHILE SMOKING. CAN CAUSE SERIOUS INJURY OR DEATH
Keep away from face and mouth to avoid breathing in.
Avoid spraying in eyes. Contents under pressure. Do not puncture or incinerate. Do not expose to heat or store at temperatures above 120°F/50°C or in enclosed places that could overheat
Do not use on broken skin. Stop use if rash or irritation occurs.
Ask a doctor before using if you have kidney disease.
USE ONLY AS DIRECTED. INTENTIONAL MISUSE BY DELIBERATELY CONCENTRATING AND INHALING THE CONTENTS CAN BE HARMFUL OR FATAL.

Help stop inhalation abuse. For information visit www.inhalant.org

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN.

Directions

Apply to underarms only. If dispenser clogs, rinse in warm water

Inactive ingredients

Butane, Cyclopentasiloxane, Hydrofluorocarbon 152a, Isobutane, PPG-14 Butyl Ether, Fragrance (Parfum), Disteardimonium Hectorite, Propane, BHT, Propylene Carbonate,Butylphenyl Methylpropional, Citronellol, Coumarin, Geraniol, Limonene, Linalool.

Questions?

Call toll-free 1-800-761-3683

Packaging

INGREDIENTS AND APPEARANCE

AXE 
apollo dry spray antiperspirant 48hr protection dry aerosol, spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64942-1565
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M)	ALUMINUM CHLOROHYDRATE	23.3 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
.BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
BUTANE (UNII: 6LV4FOR43R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
1,1-DIFLUOROETHANE (UNII: 0B1U8K2ME0)
PPG-14 BUTYL ETHER (UNII: R199TJT95T)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
PROPANE (UNII: T75W9911L6)
ISOBUTANE (UNII: BXR49TP611)
BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
COUMARIN (UNII: A4VZ22K1WT)
GERANIOL (UNII: L837108USY)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
LINALOOL, (+/-)- (UNII: D81QY6I88E)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64942-1565-1	28 g in 1 CAN; Type 0: Not a Combination Product	01/31/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part350	01/31/2018

Labeler - Conopco Inc. d/b/a/ Unilever (001375088)