FDA.reportPublic FDA data

Degree Men Black + White Dry Spray Antiperspirant

Manufacturer
Conopco Inc. d/b/a/ Unilever
Effective date
2020-10-02
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:30:51

Label at a glance#

ProductDegree Men Black and White Dry Antiperspirant
Active ingredientALUMINUM CHLOROHYDRATE
Label structure10 sections

Indications and uses

 Reduces underarm wetness

Dosage and administration

For underarm use only

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Chlorohydrate (20.2 %)

Purpose

OTC - PURPOSE SECTION

antiperspirant

Uses

INDICATIONS & USAGE SECTION

  •  Reduces underarm wetness

Warnings

WARNINGS SECTION

  • 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

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, Fragrance (Parfum), Propane, BHT, Caprylic/Capric Triglyceride, Sodium Starch Octenylsuccinate, Propylene Carbonate, Maltodextrin, Hydrated Silica, Hydrolyzed Corn Starch, Gelatin Crosspolymer, Silica, Cellulose Gum, Sodium Benzoate.

Questions?

OTC - QUESTIONS SECTION

Call toll-free 1-866-334-7331

SPL UNCLASSIFIED SECTION

DRY SPRAY

ANTI YELLOW STAINS & WHITE MARKS

48H ANTIPERSPIRANT

MOTION ACTIVATED PROTECTION

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64942-1442-12025-01-30C16284748780-19d75b9d0-4cba-f424-e053-dadaa90a57ceDegree Men Black + White Dry Spray Antiperspirant
64942-1442-12020-09-29C16284748780-19d75b9d0-4cba-f424-e053-dadaa90a57ceDegree Men Black + White Dry Spray Antiperspirant
64942-1442-12020-01-31C16284748780-19d75b9d0-4cba-f424-e053-dadaa90a57ceDegree Men Black + White Dry Spray Antiperspirant

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64942-1442-1Degree MenBlack and White Dry Antiperspirant107 g in 1 CANAEROSOL, SPRAY1073

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64942-1442DEGREE MEN BLACK AND WHITE DRY ANTIPERSPIRANT (ALUMINUM CHLOROHYDRATE) AEROSOL, SPRAY [CONOPCO INC. D/B/A/ UNILEVER]3Legacy NDC, 1 package rows20201003_171ebd23-da1d-49b4-8fb4-3c56771e05e1.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
64942-144264942-1442-1

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
b0b79a50-67fc-76d6-e053-2a95a90afb66171ebd23-da1d-49b4-8fb4-3c56771e05e12020-10-02WarningsExact identifier
spl id: b0b79a50-67fc-76d6-e053-2a95a90afb66
spl set id: 171ebd23-da1d-49b4-8fb4-3c56771e05e1

Reported adverse events (FAERS/openFDA)#

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