Dove

Manufacturer
Conopco Inc. d/b/a Unilever
Effective date
2024-10-24
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 00:29:50

Label at a glance#

ProductDove Clinical Protection Skin Renew Antiperspirant
Active ingredientALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Aluminum Zirconium Tetrachlorohydrex GLY (20%)

OTC - PURPOSE SECTION

Purpose
anti-perspirant

INDICATIONS & USAGE SECTION

Uses
•
reduces underarm wetness
• extra effective

WARNINGS SECTION

Warnings
• 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.

DOSAGE & ADMINISTRATION SECTION

Directions
• apply to underarms only
• before bed, apply two clicks of product to each underarm

INACTIVE INGREDIENT SECTION

Inactive ingredients
Cyclopentasiloxane, Dimethicone, Paraffin, Microcrystalline Wax, Fragrance (Parfum), Silica, Helianthus Annuus  (Sunflower) Seed Oil, Dimethicone Crosspolymer, Glycine Soja (Soybean) Oil, Calendula Officinalis Flower Extract, BHT.

OTC - QUESTIONS SECTION

Questions?  Call toll-free 1-800-761-3683

1.7 oz PDP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DVClinSkinRenewPDPDVClinSkinRenewPDP

1.7 oz Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DVClinSkinRenewCartonDVClinSkinRenewCarton

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
baf7f49c-75b6-496b-a00e-8e766a8e4f03Product name120210127
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64942-1439-1DoveClinical Protection Skin Renew Antiperspirant48 g in 1 CONTAINERSTICK485
64942-1439-2DoveClinical Protection Skin Renew Antiperspirant1 in 1 CARTONSTICK15
64942-1439-3DoveClinical Protection Skin Renew Antiperspirant14 g in 1 CONTAINERSTICK145
64942-1439-4DoveClinical Protection Skin Renew Antiperspirant1 in 1 CARTONSTICK15
64942-1439-5DoveClinical Protection Skin Renew Antiperspirant62 g in 1 CONTAINERSTICK625
64942-1439-6DoveClinical Protection Skin Renew Antiperspirant1 in 1 CARTONSTICK15

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64942-1439DOVE CLINICAL PROTECTION SKIN RENEW ANTIPERSPIRANT (ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY) STICK [CONOPCO INC. D/B/A UNILEVER]5Current NDC, Legacy NDC, 6 package rows20241027_448c03c9-930c-4145-bcb3-751553dc356b.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64942-143964942-1439-1, 64942-1439-2, 64942-1439-3, 64942-1439-4, 64942-1439-5, 64942-1439-6

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

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
Dove Clinical Protection Skin Renew AntiperspirantALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLYConopco Inc. d/b/a Unilever448c03c9-930c-4145-bcb3-751553dc356b2024-10-24WarningsExact identifier
ndc (package): 64942-1439-6
ndc (package): 64942-1439-1
ndc (package): 64942-1439-5
ndc (package): 64942-1439-2
ndc (package): 64942-1439-3
ndc (package): 64942-1439-4
ndc (product): 64942-1439
ndc11 (package): 64942143904
ndc11 (package): 64942143905
ndc11 (package): 64942143901
ndc11 (package): 64942143906
ndc11 (package): 64942143903
ndc11 (package): 64942143902
spl id: 253be68a-9664-b800-e063-6294a90ad488
spl set id: 448c03c9-930c-4145-bcb3-751553dc356b

Reported adverse events (FAERS/openFDA)#

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