FDA.reportPublic FDA data

Dove

Manufacturer
Conopco, Inc. d/b/a/ Unilever
Effective date
2021-03-10
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:38:54

Label at a glance#

ProductDove Dermacare Scalp Dryness and Itch Relief Anti-Dandruff
Active ingredientPYRITHIONE ZINC
Label structure10 sections

Dosage and administration

For best results use at least twice per week or as directed by a doctor. Massage into scalp and hair. Rinse.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Pyrithione Zinc (1.0%)

Purpose

OTC - PURPOSE SECTION

Anti-dandruff

Use

INDICATIONS & USAGE SECTION

Helps prevent and control recurrence of itching, flaking and irritation associated with dandruff.

Warning

WARNINGS SECTION

For external use only
When using this product Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.
Stop use and ask a doctor if Condition worsens or does not improve after regular use of this product as directed.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this and all drugs out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

For best results use at least twice per week or as directed by a doctor. Massage into scalp and hair. Rinse.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Sodium Laureth Sulfate, Cocamidopropyl Betaine, Sodium Chloride, Cocos Nucifera (Coconut) Oil, Butyrospermum Parkii (Shea) Butter, Carbomer, Fragrance (Parfum), Dimethiconol, DMDM Hydantoin, Citric Acid, Glycerin, PPG-9, Zinc Sulfate, Guar Hydroxypropyltrimonium Chloride, TEA-Dodecylbenzenesulfonate, Butylene Glycol, Iodopropynyl Butylcarbamate, Methylchloroisothiazolinone, Methylisothiazolinone

Questions, comments?

OTC - QUESTIONS SECTION

Call 1-800-761-3683

SPL UNCLASSIFIED SECTION

Gently cleanses & soothes itchy, dry scalp
For smooth, less frizzy hair
FLAKE FREE* + pH BALANCED
The solution that nourishes the scalp and relieves it from irritation

  • Leaves hair flake free*
  • Hydrates dry scalp
  • Soothes itchy scalp
  • Coconut & Shea butter indulgent scent
  • For smooth, less frizzy hair

*No visible flakes with regular use

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
209884zinc pyrithione 1 % Medicated ShampooPSN3
209884zinc pyrithione 10 MG/ML Medicated ShampooSCD3
209884zinc pyrithione 1 % Medicated ConditionerSY3
209884zinc pyrithione 1 % Medicated ShampooSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64942-1487-12025-01-30C16284748780-19d75b9d0-63be-f424-e053-dadaa90a57ceDove Dermacare Scalp Dryness and Itch Relief Anti-Dandruff Shampoo
64942-1487-22025-01-30C16284748780-19d75b9d0-63be-f424-e053-dadaa90a57ceDove Dermacare Scalp Dryness and Itch Relief Anti-Dandruff Shampoo
64942-1487-12021-03-10C16284748780-19d75b9d0-63be-f424-e053-dadaa90a57ceDove Dermacare Scalp Dryness and Itch Relief Anti-Dandruff Shampoo
64942-1487-22021-03-10C16284748780-19d75b9d0-63be-f424-e053-dadaa90a57ceDove Dermacare Scalp Dryness and Itch Relief Anti-Dandruff Shampoo
64942-1487-12020-01-31C16284748780-19d75b9d0-63be-f424-e053-dadaa90a57ceDove Dermacare Scalp Dryness and Itch Relief Anti-Dandruff Shampoo
64942-1487-22020-01-31C16284748780-19d75b9d0-63be-f424-e053-dadaa90a57ceDove Dermacare Scalp Dryness and Itch Relief Anti-Dandruff Shampoo

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64942-1487-1DoveDermacare Scalp Dryness and Itch Relief Anti-Dandruff355 mL in 1 CONTAINERSHAMPOO3553
64942-1487-2DoveDermacare Scalp Dryness and Itch Relief Anti-Dandruff53 mL in 1 CONTAINERSHAMPOO533

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64942-1487DOVE DERMACARE SCALP DRYNESS AND ITCH RELIEF ANTI-DANDRUFF (PYRITHIONE ZINC) SHAMPOO [CONOPCO, INC. D/B/A/ UNILEVER]3Legacy NDC, 2 package rows20210312_39487ac0-4690-4da1-8c45-e6ea2d72eac0.zip

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64942-148764942-1487-1, 64942-1487-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
SODIUM LAURETH-3 SULFATEBPV390UAP0IACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
SODIUM CHLORIDE451W47IQ8XIACT
COCONUT OILQ9L0O73W7LIACT
SHEA BUTTERK49155WL9YIACT
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED)4Q93RCW27EIACT
DIMETHICONOL (40 CST)343C7U75XWIACT
DMDM HYDANTOINBYR0546TOWIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
GLYCERINPDC6A3C0OXIACT
PPG-9I29VQH0G0BIACT
ZINC SULFATE, UNSPECIFIED FORM89DS0H96TBIACT
GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE)B16G315W7AIACT
TRIETHANOLAMINE DODECYLBENZENESULFONATE8HM7ZD48HNIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
IODOPROPYNYL BUTYLCARBAMATE603P14DHEBIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
PYRITHIONE ZINCR953O2RHZ5ACTIB

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
bd35f98d-742e-0b65-e053-2a95a90a49f339487ac0-4690-4da1-8c45-e6ea2d72eac02021-03-10WarningsExact identifier
spl id: bd35f98d-742e-0b65-e053-2a95a90a49f3
spl set id: 39487ac0-4690-4da1-8c45-e6ea2d72eac0

Reported adverse events (FAERS/openFDA)#

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