FDA.reportPublic FDA data

Degree MotionSense Ultraclear Black and White Dry Spray Antiperspirant

Manufacturer
Conopco Inc. d/b/a Unilever | Unilever Manufacturera S. de R.L. de C.V.
Effective date
2020-09-28
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:30:38

Label at a glance#

ProductDegree
Active ingredientALUMINUM CHLOROHYDRATE
Label structure9 sections

Indications and uses

reduces underarm wetness

Dosage and administration

For underarm use only

Label contents#

Full prescribing information#

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

DESCRIPTION SECTION

Degree MotionSense Ultraclear Black and White Dry Spray Antiperspirant

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient:

Aluminum Chlorohydrate (20.2%)

Purpose:

OTC - PURPOSE SECTION

antiperspirant

Uses

INDICATIONS & USAGE SECTION

reduces underarm wetness

Warnings

WARNINGS SECTION

• 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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

• KEEP OUT OF REACH OF CHILDREN

Directions

DOSAGE & ADMINISTRATION SECTION

For underarm use only

Inactive ingredients

INACTIVE INGREDIENT SECTION

Butane, Cyclopentasiloxane, Hydrofluorocarbon 152a, Isobutane, PPG-14 Butyl Ether, Disteardimonium Hectorite, Propane, Fragrance (Parfum), BHT, Propylene Carbonate, Caprylic/Capric Triglyceride, Sodium Starch Octenylsuccinate, Maltodextrin, Hydrated Silica, Hydrolyzed Corn Starch, Gelatin Crosspolymer, Silica, Cellulose Gum, Sodium Benzoate, Alpha-Isomethyl Lonone, Benzyl Alcohol, Benzyl Salicylate, Butylphenyl Methylpropional, Citronellol, Hexyl Cinnamal, Hydroxycitronellal, Limonene, Linalool.

Questions?

OTC - QUESTIONS SECTION

Call toll-free 1-866-334-7331

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DegreeUltraclearBlackWhiteDrySprayAPDegreeUltraclearBlackWhiteDrySprayAP

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64942-1568-12025-01-30C16284748780-19d75b9d0-3cca-f424-e053-dadaa90a57ceDegree MotionSense Ultraclear Black and White Dry Spray Antiperspirant
64942-1568-12020-09-30C16284748780-19d75b9d0-3cca-f424-e053-dadaa90a57ceDegree MotionSense Ultraclear Black and White Dry Spray Antiperspirant
64942-1568-12020-01-31C16284748780-19d75b9d0-3cca-f424-e053-dadaa90a57ceDegree MotionSense Ultraclear Black and White Dry Spray Antiperspirant

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64942-1568-1Degree28 g in 1 CANAEROSOL, SPRAY282

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64942-1568DEGREE (MOTIONSENSE ULTRACLEAR BLACK AND WHITE DRY SPRAY ANTIPERSPIRANT) AEROSOL, SPRAY [CONOPCO INC. D/B/A UNILEVER]2Legacy NDC, 1 package rows20201001_6418350c-b5bf-badb-e053-2991aa0a4db6.zip

Products#

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

DailyMed product names page 1 of 1 · 29 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64942-156864942-1568-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 26 matching rows.

Name, UNII, Kind table
NameUNIIKind
LINALOOL, (+/-)-D81QY6I88EIACT
MALTODEXTRIN7CVR7L4A2DIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORMK679OBS311IACT
SODIUM BENZOATEOJ245FE5EUIACT
BENZYL ALCOHOLLKG8494WBHIACT
ISOMETHYL-.ALPHA.-IONONE9XP4LC555BIACT
BENZYL SALICYLATEWAO5MNK9TUIACT
BUTYLPHENYL METHYLPROPIONALT7540GJV69IACT
.BETA.-CITRONELLOL, (R)-P01OUT964KIACT
LIMONENE, (+)-GFD7C86Q1WIACT
BUTANE6LV4FOR43RIACT
1,1-DIFLUOROETHANE0B1U8K2ME0IACT
CYCLOMETHICONE 50THT5PCI0RIACT
ISOBUTANEBXR49TP611IACT
DISTEARDIMONIUM HECTORITEX687XDK09LIACT
PROPANET75W9911L6IACT
PROPYLENE CARBONATE8D08K3S51EIACT
HYDRATED SILICAY6O7T4G8P9IACT
STARCH, CORNO8232NY3SJIACT
PPG-14 BUTYL ETHERR199TJT95TIACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
.ALPHA.-HEXYLCINNAMALDEHYDE7X6O37OK2IIACT
HYDROXYCITRONELLAL8SQ0VA4YURIACT
ALUMINUM CHLOROHYDRATEHPN8MZW13MACTIB

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
b05fcebb-d028-c117-e053-2995a90a10646418350c-b5bf-badb-e053-2991aa0a4db62020-09-28WarningsExact identifier
spl id: b05fcebb-d028-c117-e053-2995a90a1064
spl set id: 6418350c-b5bf-badb-e053-2991aa0a4db6

Reported adverse events (FAERS/openFDA)#

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