FDA.reportPublic FDA data

Degree

Manufacturer
Conopco, Inc. d/b/a Unilever
Effective date
2022-12-07
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:52:11

Label at a glance#

ProductDegree
Active ingredientALUMINUM CHLOROHYDRATE
Label structure10 sections

Indications and uses

reduces underarm wetness

Dosage and administration

apply to underarms only

Label contents#

Full prescribing information#

DEGREE ALL DAY PROTECTION TO MOVE MORE DRY SPRAY DAISY POWER ANTIPERSPIRANT DEODORANT - aluminum chlorohydrate aerosol, spray

DESCRIPTION SECTION

Degree All Day Protection to Move More Dry Spray Daisy Power Antiperspirant Deodorant

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. 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

apply to underarms only

Inactive ingredients

INACTIVE INGREDIENT SECTION

Butane, Hydrofluorocarbon 152a, Cyclopentasiloxane, Isobutane, PPG-14 Butyl Ether, Helianthus Annuus (Sunflower) Seed Oil, Disteardimonium Hectorite, C12-15 Alkyl Benzoate, Fragrance (Parfum), Propane, BHT, Octyldodecanol, Propylene Carbonate, Dimethiconol, Tocopheryl Acetate.

Questions?

OTC - QUESTIONS SECTION

Call toll-free 1-866-334-7331

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DegreeDaisyPowerDrySprayDegreeDaisyPowerDrySpray

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64942-1647-12025-01-30C16284748780-1ba0f9c33-1dcc-a910-e053-dadaa90a0b85Degree All Day Protection to Move More Dry Spray Daisy Power Antiperspirant Deodorant
64942-1647-12021-07-30C16284748780-1ba0f9c33-1dcc-a910-e053-dadaa90a0b85Degree All Day Protection to Move More Dry Spray Daisy Power Antiperspirant Deodorant
64942-1647-12021-01-29C16284748780-1ba0f9c33-1dcc-a910-e053-dadaa90a0b85Degree All Day Protection to Move More Dry Spray Daisy Power Antiperspirant Deodorant

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64942-1647-1Degree107 g in 1 CANAEROSOL, SPRAY1073

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64942-1647DEGREE (ALUMINUM CHLOROHYDRATE) AEROSOL, SPRAY [CONOPCO, INC. D/B/A UNILEVER]3Legacy NDC, 1 package rows20221208_8a2f32ae-cbba-4fc0-e053-2995a90ab374.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64942-164764942-1647-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
CYCLOMETHICONE 50THT5PCI0RIACT
PPG-14 BUTYL ETHERR199TJT95TIACT
BUTANE6LV4FOR43RIACT
1,1-DIFLUOROETHANE0B1U8K2ME0IACT
ISOBUTANEBXR49TP611IACT
SUNFLOWER OIL3W1JG795YIIACT
DISTEARDIMONIUM HECTORITEX687XDK09LIACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
PROPANET75W9911L6IACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
OCTYLDODECANOL461N1O614YIACT
PROPYLENE CARBONATE8D08K3S51EIACT
DIMETHICONOL (41 MPA.S)343C7U75XWIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
ALUMINUM CHLOROHYDRATEHPN8MZW13MACTIB

Source Document#

Source XML · Source PDF

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
ef3fc9c5-9013-aef9-e053-2995a90ad42d8a2f32ae-cbba-4fc0-e053-2995a90ab3742022-12-07WarningsExact identifier
spl id: ef3fc9c5-9013-aef9-e053-2995a90ad42d
spl set id: 8a2f32ae-cbba-4fc0-e053-2995a90ab374

Reported adverse events (FAERS/openFDA)#

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