FDA.reportPublic FDA data

Suave

Manufacturer
Conopco Inc. d/b/a Unilever
Effective date
2021-03-12
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:38:57

Label at a glance#

ProductSuave Men 2 in 1 Pure Power Antidandruff
Active ingredientPYRITHIONE ZINC
Label structure8 sections

Dosage and administration

• wet hair, lather, rinse, and repeat. • for best results, use at least twice a week or as directed by a doctor.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Pyrithione Zinc (1.0%)

Purpose

OTC - PURPOSE SECTION

Antidandruff

Use

INDICATIONS & USAGE SECTION

controls scalp itching and flaking associated with dandruff.

Warnings

WARNINGS SECTION


• For external use only

OTC - WHEN USING SECTION

• When using this product avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

• 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 out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• wet hair, lather, rinse, and repeat.

• for best results, use at least twice a week or as directed by a doctor.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Sodium Laureth Sulfate, Cocamidopropyl Betaine, Sodium Chloride, Carbomer, Fragrance (Parfum), Dimethiconol, DMDM Hydantoin, Citric Acid, Zinc Sulfate, PPG-9, Guar Hydroxypropyltrimonium Chloride, TEA-Dodecylbenzenesulfonate, Butylene Glycol, Iodopropynyl Butylcarbamate, Methylchloroisothiazolinone, Methylisothiazolinone.

Questions or comments?

OTC - QUESTIONS SECTION

Call us at 1-800-782-8301

Mon - Fri 8:30-6:00 pm EST

Package

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Suave Power Anti-Dandruff SH CDSuave Power Anti-Dandruff SH CD

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
209884zinc pyrithione 1 % Medicated ShampooPSN2
209884zinc pyrithione 10 MG/ML Medicated ShampooSCD2
209884zinc pyrithione 1 % Medicated ConditionerSY2
209884zinc pyrithione 1 % Medicated ShampooSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64942-1437-12024-01-30C16284748780-19d75b9cf-f58d-f424-e053-dadaa90a57ceSuave Men 2 in 1 Pure Power Anti Dandruff Shampoo and Conditioner
64942-1437-22024-01-30C16284748780-19d75b9cf-f58d-f424-e053-dadaa90a57ceSuave Men 2 in 1 Pure Power Anti Dandruff Shampoo and Conditioner
64942-1437-12021-03-12C16284748780-19d75b9cf-f58d-f424-e053-dadaa90a57ceSuave Men 2 in 1 Pure Power Anti Dandruff Shampoo and Conditioner
64942-1437-22021-03-12C16284748780-19d75b9cf-f58d-f424-e053-dadaa90a57ceSuave Men 2 in 1 Pure Power Anti Dandruff Shampoo and Conditioner
64942-1437-12020-01-31C16284748780-19d75b9cf-f58d-f424-e053-dadaa90a57ceSuave Men 2 in 1 Pure Power Anti Dandruff Shampoo and Conditioner
64942-1437-22020-01-31C16284748780-19d75b9cf-f58d-f424-e053-dadaa90a57ceSuave Men 2 in 1 Pure Power Anti Dandruff Shampoo and Conditioner

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64942-1437-1SuaveMen 2 in 1 Pure Power Antidandruff828 mL in 1 CONTAINERSHAMPOO8282
64942-1437-2SuaveMen 2 in 1 Pure Power Antidandruff373 mL in 1 CONTAINERSHAMPOO3732

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64942-1437SUAVE MEN 2 IN 1 PURE POWER ANTIDANDRUFF (PYRITHIONE ZINC) SHAMPOO [CONOPCO INC. D/B/A UNILEVER]2Legacy NDC, 2 package rows20210313_4d8adf15-c098-4b61-9bd9-cc014612cc63.zip

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64942-143764942-1437-1, 64942-1437-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Name, UNII, Kind table
NameUNIIKind
ZINC SULFATE89DS0H96TBIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
WATER059QF0KO0RIACT
SODIUM LAURETH SULFATEBPV390UAP0IACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
SODIUM CHLORIDE451W47IQ8XIACT
DMDM HYDANTOINBYR0546TOWIACT
TRIETHANOLAMINE DODECYLBENZENESULFONATE8HM7ZD48HNIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
PPG-9I29VQH0G0BIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE)B16G315W7AIACT
DIMETHICONOL (41 MPA.S)343C7U75XWIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
IODOPROPYNYL BUTYLCARBAMATE603P14DHEBIACT
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
bd57e478-f051-20e7-e053-2995a90a5bf14d8adf15-c098-4b61-9bd9-cc014612cc632021-03-12WarningsExact identifier
spl id: bd57e478-f051-20e7-e053-2995a90a5bf1
spl set id: 4d8adf15-c098-4b61-9bd9-cc014612cc63

Reported adverse events (FAERS/openFDA)#

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