Degree Clinical Protection Sheer Powder

Manufacturer: Conopco Inc. d/b/a Unilever
Effective date: 2010-06-08
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 22:24:48

Label at a glance#

ProductDegree Clinical Protection Sheer Powder Antiperspirant and Deodorant

Active ingredientAluminum Zirconium Tetrachlorohydrex GLY

Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient Purpose

Aluminum Zirconium Tetrachlorohydrex GLY (20%).................anti-perspirant

WARNINGS SECTION

Warnings For External Use only

INACTIVE INGREDIENT SECTION

Cyclopentasiloxane, Dimethicone, Microcrystalline Wax, C18-36 Acid Triglyceride, Fragrance (Parfum), Silica, Zea Mays (Corn) Starch, Dimethicone Crosspolymer, BHT.

OTC - QUESTIONS SECTION

Questions? Call toll-free 1-866-DEGREE1

OTC - DO NOT USE SECTION

Do not use on broken skin

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have kidney disease

OTC - STOP USE SECTION

Stop use if rash or irritation occurs

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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDP front 1.7oz

Degree Clinical Sheer Powder 1.7 front PDP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDP 1.7 oz back

Degree Clinical Sheer Powder 1.7 back PDP

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
64942-1035-2	2020-01-31	C162847	48780-1	9d75b9d0-057d-f424-e053-dadaa90a57ce	PDP Degree Clinical Protection Sheer Powder IS AP and Deod., and drug facts
64942-1035-4	2020-01-31	C162847	48780-1	9d75b9d0-057d-f424-e053-dadaa90a57ce	PDP Degree Clinical Protection Sheer Powder IS AP and Deod., and drug facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
64942-1035-1	Degree Clinical Protection Sheer PowderAntiperspirant and Deodorant	48 g in 1 CONTAINER	STICK	48	2
64942-1035-2	Degree Clinical Protection Sheer PowderAntiperspirant and Deodorant	1 in 1 CARTON	STICK	1	2
64942-1035-3	Degree Clinical Protection Sheer PowderAntiperspirant and Deodorant	14 g in 1 CONTAINER	STICK	14	2
64942-1035-4	Degree Clinical Protection Sheer PowderAntiperspirant and Deodorant	1 in 1 CARTON	STICK	1	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
64942-1035	DEGREE CLINICAL PROTECTION SHEER POWDER ANTIPERSPIRANT AND DEODORANT (ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY) STICK [CONOPCO INC. D/B/A UNILEVER]	2	Legacy NDC, 4 package rows	20100611_58c8b1fd-cee9-41e7-a455-79e88bd03db9.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version	Uploaded
Aluminum Zirconium Tetrachlorohydrex GLY	ACTIVE INGREDIENT	8O386558JE	2
Aluminum cation	ACTIVE MOIETY	3XHB1D032B	2

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

Degree Clinical Protection Sheer Powder Antiperspirant and Deodorant
Aluminum Zirconium Tetrachlorohydrex GLY
Aluminum cation

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
64942-1035	64942-1035-1, 64942-1035-2, 64942-1035-3, 64942-1035-4

Ingredients#

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

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

Name, UNII, Kind table
Name	UNII	Kind
Aluminum Zirconium Tetrachlorohydrex GLY	8O386558JE	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
f5036177-5219-4a5e-8d89-75c5c8db45b8			58c8b1fd-cee9-41e7-a455-79e88bd03db9	2010-06-08	Warnings	Exact identifier spl id: f5036177-5219-4a5e-8d89-75c5c8db45b8 spl set id: 58c8b1fd-cee9-41e7-a455-79e88bd03db9

Reported adverse events (FAERS/openFDA)#

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