FDA.reportPublic FDA data

Degree for Women Motionsense Active Shield 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
3
Source
full-release
Hydrated at
2026-05-31 23:30:37

Label at a glance#

ProductDegree for Women Motionsense Active Shield Antiperspirant
Active ingredientALUMINUM CHLOROHYDRATE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient:

Aluminum Chlorohydrate (23.3%)

OTC - PURPOSE SECTION

Purpose:

anti-perspirant

INDICATIONS & USAGE SECTION

Uses:
· reduces underarm wetness

WARNINGS SECTION

WARNINGS:

• 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 degrees F/50 degrees 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

DOSAGE & ADMINISTRATION SECTION

Directions:

For underarm use only.

INACTIVE INGREDIENT SECTION

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

OTC - QUESTIONS SECTION

Questions? Call toll-free 1-866-334-7331

3.8 oz PDP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DegreeMSWomenActiveShieldAPSprayPDPDegreeMSWomenActiveShieldAPSprayPDP

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64942-1408-12025-01-30C16284748780-19d75b9d0-4c63-f424-e053-dadaa90a57ceDegree for Women Motionsense Active Shield Dry Spray Antiperspirant
64942-1408-22025-01-30C16284748780-19d75b9d0-4c63-f424-e053-dadaa90a57ceDegree for Women Motionsense Active Shield Dry Spray Antiperspirant
64942-1408-12020-09-30C16284748780-19d75b9d0-4c63-f424-e053-dadaa90a57ceDegree for Women Motionsense Active Shield Dry Spray Antiperspirant
64942-1408-22020-09-30C16284748780-19d75b9d0-4c63-f424-e053-dadaa90a57ceDegree for Women Motionsense Active Shield Dry Spray Antiperspirant
64942-1408-12020-01-31C16284748780-19d75b9d0-4c63-f424-e053-dadaa90a57ceDegree for Women Motionsense Active Shield Dry Spray Antiperspirant
64942-1408-22020-01-31C16284748780-19d75b9d0-4c63-f424-e053-dadaa90a57ceDegree for Women Motionsense Active Shield Dry Spray Antiperspirant

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64942-1408-1Degreefor Women Motionsense Active Shield Antiperspirant107 g in 1 CANAEROSOL, SPRAY1073
64942-1408-2Degreefor Women Motionsense Active Shield Antiperspirant28 g in 1 CANAEROSOL, SPRAY283

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64942-1408DEGREE FOR WOMEN MOTIONSENSE ACTIVE SHIELD ANTIPERSPIRANT (ALUMINUM CHLOROHYDRATE) AEROSOL, SPRAY [CONOPCO INC. D/B/A UNILEVER]3Legacy NDC, 2 package rows20201001_5d045214-ff5d-4e15-bad0-5c1578ddeafa.zip

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64942-140864942-1408-1, 64942-1408-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
BUTANE6LV4FOR43RIACT
1,1-DIFLUOROETHANE0B1U8K2ME0IACT
CYCLOMETHICONE 50THT5PCI0RIACT
ISOBUTANEBXR49TP611IACT
PPG-14 BUTYL ETHERR199TJT95TIACT
DISTEARDIMONIUM HECTORITEX687XDK09LIACT
PROPANET75W9911L6IACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
PROPYLENE CARBONATE8D08K3S51EIACT
HYDRATED SILICAY6O7T4G8P9IACT
MALTODEXTRIN7CVR7L4A2DIACT
SODIUM BENZOATEOJ245FE5EUIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
CARBOXYMETHYLCELLULOSE SODIUMK679OBS311IACT
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
b05f9b1f-b3f0-6b86-e053-2a95a90abc005d045214-ff5d-4e15-bad0-5c1578ddeafa2020-09-28WarningsExact identifier
spl id: b05f9b1f-b3f0-6b86-e053-2a95a90abc00
spl set id: 5d045214-ff5d-4e15-bad0-5c1578ddeafa

Reported adverse events (FAERS/openFDA)#

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