DEGREE- men motionsense ultraclear black and white dry spray antiperspirant aerosol, spray 
Conopco Inc. d/b/a Unilever

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Degree Men MotionSense Ultraclear Black and White Dry Spray Antiperspirant

DEGREE MEN MOTIONSENSE ULTRACLEAR BLACK AND WHITE DRY SPRAY ANTIPERSPIRANT - aluminum chlorohydrate aerosol, spray

Degree Men MotionSense Ultraclear Black and White Dry Spray Antiperspirant

Drug Facts

Active Ingredient:

Aluminum Chlorohydrate (20.2%)

Purpose:

antiperspirant

Uses

reduces underarm wetness

Warnings

FLAMMABLE UNTILFULLY DRY. 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

Directions

For underarm use only

Inactive ingredients

Butane, Cyclopentasiloxane, Hydrofluorocarbon 152a, Isobutane, PPG-14 Butyl Ether, Disteardimonium Hectorite, Fragrance (Parfum), Propane, BHT, Propylene Carbonate, Caprylic/Capric Triglyceride, Sodium Starch Octenylsuccinate, Maltodextrin, Hydrated Silica, Hydrolyzed Corn Starch, Gelatin Crosspolymer, Silica, Cellulose Gum, Sodium Benzoate, Citral, Limonene, Linalool.

Questions?

Call toll-free 1-866-334-7331

Packaging

DegreeMenUltraclearBlackWhiteDrySprayAP

DEGREE 
men motionsense ultraclear black and white dry spray antiperspirant aerosol, spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-1569
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE20.2 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
CITRAL (UNII: T7EU0O9VPP)  
LINALOOL, (+/-)- (UNII: D81QY6I88E)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
LIMONENE, (+)- (UNII: GFD7C86Q1W)  
BUTANE (UNII: 6LV4FOR43R)  
1,1-DIFLUOROETHANE (UNII: 0B1U8K2ME0)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
ISOBUTANE (UNII: BXR49TP611)  
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
PROPANE (UNII: T75W9911L6)  
PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
HYDRATED SILICA (UNII: Y6O7T4G8P9)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
PPG-14 BUTYL ETHER (UNII: R199TJT95T)  
STARCH, CORN (UNII: O8232NY3SJ)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:64942-1569-128 g in 1 CAN; Type 0: Not a Combination Product01/31/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35001/31/2018
Labeler - Conopco Inc. d/b/a Unilever (001375088)

Revised: 9/2020
Document Id: b06267cd-678a-f0da-e053-2995a90af30c
Set id: 641d6e42-b5f5-34a4-e053-2a91aa0acef9
Version: 2
Effective Time: 20200928
 
Conopco Inc. d/b/a Unilever