Dove Ultimate Go Fresh Refreshing

Manufacturer: Conopco Inc. d/b/a Unilever | Unilever Raeford HPCNA
Effective date: 2010-06-08
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:24:43

Label at a glance#

ProductDove Ultimate Go Fresh Refreshing Antiperspirant and Deodorant

Active ingredientAluminum Zirconium Tetrachlorohydrex GLY

Label structure10 sections

Contacts and useful links#

PhoneLabel contact1-800-761-DOVE

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient Purpose

Aluminum Zirconium Tetrachlorohydrex GLY(14.8%)............anti-perspirant

WARNINGS SECTION

Warning
For external use only

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.

INACTIVE INGREDIENT SECTION

Inactive ingredients

Cyclopentasiloxane, Stearyl Alcohol, C12-15 Alkyl Benzoate, PPG-14 Butyl Ether, Hydrogenated Castor Oil, Dimethicone, Polyethylene, Fragrance (Parfum), Steareth-100, Helianthus Annuus (Sunflower) Seed Oil, BHT.

OTC - QUESTIONS SECTION

Questions?

Call toll-free 1-800-761-DOVE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDP 2.6 oz front

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDP 2.6 oz back

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
64942-1052-1	2020-01-31	C162847	48780-1	9d75b9cf-d3be-f424-e053-dadaa90a57ce	Dove Ultimate Go Fresh Refreshing Antiperspirant and Deodorant PDP and drug facts
64942-1052-2	2020-01-31	C162847	48780-1	9d75b9cf-d3be-f424-e053-dadaa90a57ce	Dove Ultimate Go Fresh Refreshing Antiperspirant and Deodorant PDP and drug facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
64942-1052-1	Dove Ultimate Go Fresh RefreshingAntiperspirant and Deodorant	74 g in 1 CONTAINER	STICK	74		1
64942-1052-2	Dove Ultimate Go Fresh RefreshingAntiperspirant and Deodorant	45 g in 1 CONTAINER	STICK	45		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
64942-1052	DOVE ULTIMATE GO FRESH REFRESHING ANTIPERSPIRANT AND DEODORANT (ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY) STICK [CONOPCO INC. D/B/A UNILEVER]	1	Legacy NDC, 2 package rows	20100608_563ab76d-a58b-4296-874d-9594e3ee6dcb.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version	Uploaded
Aluminum Zirconium Tetrachlorohydrex GLY	ACTIVE INGREDIENT	8O386558JE	1
Aluminum cation	ACTIVE MOIETY	3XHB1D032B	1

Products#

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

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

Dove Ultimate Go Fresh Refreshing Antiperspirant and Deodorant
Aluminum Zirconium Tetrachlorohydrex GLY
Aluminum cation

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
64942-1052	64942-1052-1, 64942-1052-2

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
798e1ec0-8e6e-4704-9581-c4d64e72eca1			563ab76d-a58b-4296-874d-9594e3ee6dcb	2010-06-08	Warnings	Exact identifier spl id: 798e1ec0-8e6e-4704-9581-c4d64e72eca1 spl set id: 563ab76d-a58b-4296-874d-9594e3ee6dcb

Reported adverse events (FAERS/openFDA)#

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