FDA.reportPublic FDA data

Degree Advanced Adventure Dry Spray 72H Antiperspirant Deodorant

Manufacturer
Conopco, Inc. d/b/a Unilever
Effective date
2026-06-05
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-06-11 05:10:22

Label at a glance#

ProductDegree
Active ingredientALUMINUM SESQUICHLOROHYDRATE
Label structure7 sections

Indications and uses

reduces underarm wetness

Dosage and administration

For underarms use only

Label contents#

Full prescribing information#

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Aluminum Sesquichlorohydrate (17.6%)

Purpose

OTC - PURPOSE SECTION

antiperspirant

Uses

INDICATIONS & USAGE SECTION



reduces underarm wetness

Directions

DOSAGE & ADMINISTRATION SECTION

For underarms use only

Inactive ingredients

INACTIVE INGREDIENT SECTION

Butane, Hydrofluorocarbon 152a, Cyclopentasiloxane, Isobutane, PPG-14 Butyl Ether, Glycine, Fragrance (Parfum), Disteardimonium Hectorite, Calcium Chloride, Propane, Sodium Starch Octenylsuccinate, BHT, Propylene Carbonate, Maltodextrin, Hydrolyzed Corn Starch Octenylsuccinate, Silica, Alpha-Isomethyl Ionone, Citral, Citronellol, Coumarin, Geraniol, Hexyl Cinnamal, Limonene, Linalool

Questions?

OTC - QUESTIONS SECTION

Call toll-free 1-866-334-7331

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabelDegree Adventure Dry Spray AP DeoDegree Adventure Dry Spray AP Deo

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64942-225864942-2258-1, 64942-2258-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Name, UNII, Kind table
NameUNIIKind
ISOMETHYL-.ALPHA.-IONONE9XP4LC555BIACT
.BETA.-CITRONELLOL, (R)-P01OUT964KIACT
LINALOOL, (+/-)-D81QY6I88EIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
ALUMINUM SESQUICHLOROHYDRATEUCN889409VACTIB
MALTODEXTRIN7CVR7L4A2DIACT
PROPYLENE CARBONATE8D08K3S51EIACT
GLYCINETE7660XO1CIACT
LIMONENE, (+)-GFD7C86Q1WIACT
ISOBUTANEBXR49TP611IACT
CITRALT7EU0O9VPPIACT
BUTANE6LV4FOR43RIACT
1,1-DIFLUOROETHANE0B1U8K2ME0IACT
CYCLOMETHICONE 50THT5PCI0RIACT
PPG-14 BUTYL ETHERR199TJT95TIACT
DISTEARDIMONIUM HECTORITEX687XDK09LIACT
CALCIUM CHLORIDEM4I0D6VV5MIACT
PROPANET75W9911L6IACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
.ALPHA.-HEXYLCINNAMALDEHYDE7X6O37OK2IIACT
COUMARINA4VZ22K1WTIACT
GERANIOLL837108USYIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12024-02-05full-release2026-06-01 00:08:17

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
DegreeADVANCED ADVENTURE DRY SPRAY 72H ANTIPERSPIRANT DEODORANTConopco, Inc. d/b/a Unilever10a67ae1-5602-40b4-e063-6394a90a58f62026-06-05WarningsExact identifier
ndc (package): 64942-2258-2
ndc (package): 64942-2258-1
ndc (product): 64942-2258
ndc11 (package): 64942225802
ndc11 (package): 64942225801
spl id: 5383c95c-5075-4674-e063-6294a90ae956
spl set id: 10a67ae1-5602-40b4-e063-6394a90a58f6

Reported adverse events (FAERS/openFDA)#

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