FDA.reportPublic FDA data

Degree

Manufacturer
Conopco Inc. d/b/a/ Unilever
Effective date
2024-05-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:14:31

Label at a glance#

ProductDegree
Active ingredientALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
Label structure9 sections

Indications and uses

reduces underarm wetness

Dosage and administration

apply to underarms only

Label contents#

Full prescribing information#

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Aluminum Zirconium Tetrachlorohydrex GLY (18.2 %)

Purpose

OTC - PURPOSE SECTION

antiperspirant

Uses

INDICATIONS & USAGE SECTION

reduces underarm wetness

Warnings

WARNINGS SECTION

• For external use only

• Do not use on broken skin. Stop use if rash or irritation occurs
• Ask a doctor before use if you have kidney disease

.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

• Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

apply to underarms only

Inactive ingredients

INACTIVE INGREDIENT SECTION

PPG-14 Butyl Ether, Cyclopentasiloxane,Stearyl Alcohol, Isopropyl Palmitate, Mineral Oil, Hydrogenated Castor Oil, PEG-8 Distearate, Fragrance (Parfum), Polyethylene, BHT, Alpha-Isomethyl Ionone, Benzyl Alcohol, Benzyl Salicylate, Citral, Citronellol, Coumarin, Limonene, Linalool

Questions?

OTC - QUESTIONS SECTION

Call toll-free 1-866-334-7331

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Degree Wild Woods AP Deo ISDegree Wild Woods AP Deo IS

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
9869efd7-d6dd-0665-5b67-53adbe6ef15eProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64942-2301-1Degree76 g in 1 CONTAINERSTICK761
64942-2301-2Degree2 in 1 CONTAINERSTICK21

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64942-2301DEGREE (WILD WOODS 48H ANTIPERSPIRANT DEODORANT) STICK [CONOPCO INC. D/B/A/ UNILEVER]1Current NDC, 2 package rows20240701_193644e7-0895-b683-e063-6394a90aeca8.zip

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64942-230164942-2301-1, 64942-2301-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
COUMARINA4VZ22K1WTIACT
LINALOOL, (+/-)-D81QY6I88EIACT
MINERAL OILT5L8T28FGPIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY8O386558JEACTIB
CYCLOMETHICONE 50THT5PCI0RIACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
PEG-8 DISTEARATE7JNC8VN07MIACT
HIGH DENSITY POLYETHYLENEUG00KM4WR7IACT
ISOPROPYL PALMITATE8CRQ2TH63MIACT
PPG-14 BUTYL ETHERR199TJT95TIACT
STEARYL ALCOHOL2KR89I4H1YIACT
.BETA.-CITRONELLOL, (R)-P01OUT964KIACT
BENZYL ALCOHOLLKG8494WBHIACT
CITRALT7EU0O9VPPIACT
BENZYL SALICYLATEWAO5MNK9TUIACT
LIMONENE, (+)-GFD7C86Q1WIACT
ISOMETHYL-.ALPHA.-IONONE9XP4LC555BIACT

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
DegreeWILD WOODS 48H ANTIPERSPIRANT DEODORANTConopco Inc. d/b/a/ Unilever193644e7-0895-b683-e063-6394a90aeca82024-05-24WarningsExact identifier
ndc (package): 64942-2301-1
ndc (package): 64942-2301-2
ndc (product): 64942-2301
ndc11 (package): 64942230102
ndc11 (package): 64942230101
spl id: 19363045-60b4-f8ab-e063-6294a90adcff
spl set id: 193644e7-0895-b683-e063-6394a90aeca8

Reported adverse events (FAERS/openFDA)#

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