NATURALTECH PURIFYING ANTI-DANDRUFF

Product NDC
64724-1017
11-digit product format
647241017
Labeler code
64724
Product ID
64724-1017_28ff9fbd-1d80-1984-e063-6294a90abb69
Type
HUMAN OTC DRUG
Nonproprietary name
PYRITHIONE ZINC
Dosage form
GEL
Route
TOPICAL
Labeler
Davines S.p.A.
Application
M032
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2012-02-29
Substance
PYRITHIONE ZINC
Active strength
.48 g/100mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product
Yes
Brand name base
NATURALTECH PURIFYING ANTI-DANDRUFF
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
PYRITHIONE ZINC.48 g/100mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
R953O2RHZ5Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1245937Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1f7e0265-0543-4ef9-addf-4d514d0eedfeAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64724-1017-1NATURALTECH PURIFYING ANTI-DANDRUFF1 in 1 CARTONGEL15
64724-1017-1NATURALTECH PURIFYING ANTI-DANDRUFF150 mL in 1 BOTTLEGEL1505

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
PYRITHIONE ZINCACTIVE INGREDIENTR953O2RHZ5NATURALTECH PURIFYING ANTI-DANDRUFF (PYRITHIONE ZINC) GEL [DAVINES S.P.A.]1
PYRITHIONE ZINCACTIVE MOIETYR953O2RHZ5NATURALTECH PURIFYING ANTI-DANDRUFF (PYRITHIONE ZINC) GEL [DAVINES S.P.A.]1
CARBOMER INTERPOLYMER TYPE A (55000 MPA.S)INACTIVE INGREDIENT59TL3WG5CONATURALTECH PURIFYING ANTI-DANDRUFF (PYRITHIONE ZINC) GEL [DAVINES S.P.A.]1
EDETATE SODIUMINACTIVE INGREDIENTMP1J8420LUNATURALTECH PURIFYING ANTI-DANDRUFF (PYRITHIONE ZINC) GEL [DAVINES S.P.A.]1
GLYCERININACTIVE INGREDIENTPDC6A3C0OXNATURALTECH PURIFYING ANTI-DANDRUFF (PYRITHIONE ZINC) GEL [DAVINES S.P.A.]1
LEVOMENOLINACTIVE INGREDIENT24WE03BX2TNATURALTECH PURIFYING ANTI-DANDRUFF (PYRITHIONE ZINC) GEL [DAVINES S.P.A.]1
LINALOOL, (+/-)-INACTIVE INGREDIENTD81QY6I88ENATURALTECH PURIFYING ANTI-DANDRUFF (PYRITHIONE ZINC) GEL [DAVINES S.P.A.]1
PENTASODIUM PENTETATEINACTIVE INGREDIENT961TOZ5L7TNATURALTECH PURIFYING ANTI-DANDRUFF (PYRITHIONE ZINC) GEL [DAVINES S.P.A.]1
PIROCTONE OLAMINEINACTIVE INGREDIENTA4V5C6R9FBNATURALTECH PURIFYING ANTI-DANDRUFF (PYRITHIONE ZINC) GEL [DAVINES S.P.A.]1
POLYSORBATE 20INACTIVE INGREDIENT7T1F30V5YHNATURALTECH PURIFYING ANTI-DANDRUFF (PYRITHIONE ZINC) GEL [DAVINES S.P.A.]1
PROPYLENE GLYCOLINACTIVE INGREDIENT6DC9Q167V3NATURALTECH PURIFYING ANTI-DANDRUFF (PYRITHIONE ZINC) GEL [DAVINES S.P.A.]1
SODIUM HYDROXIDEINACTIVE INGREDIENT55X04QC32INATURALTECH PURIFYING ANTI-DANDRUFF (PYRITHIONE ZINC) GEL [DAVINES S.P.A.]1
TARAXACUM OFFICINALEINACTIVE INGREDIENT39981FM375NATURALTECH PURIFYING ANTI-DANDRUFF (PYRITHIONE ZINC) GEL [DAVINES S.P.A.]1
TOCOPHEROLINACTIVE INGREDIENTR0ZB2556P8NATURALTECH PURIFYING ANTI-DANDRUFF (PYRITHIONE ZINC) GEL [DAVINES S.P.A.]1
WATERINACTIVE INGREDIENT059QF0KO0RNATURALTECH PURIFYING ANTI-DANDRUFF (PYRITHIONE ZINC) GEL [DAVINES S.P.A.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64724-1017NATURALTECH PURIFYING ANTI-DANDRUFF (PYRITHIONE ZINC) GEL [DAVINES S.P.A.]5Current NDC, Legacy NDC, 2 package rows20241213_1f7e0265-0543-4ef9-addf-4d514d0eedfe.zip

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 2 of 31 · 615 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
apgwgzminoxidil2%MINOXIDILGuangdong Jiaoyu Biotechnology Co., Ltd5957c990-e274-6278-e063-6394a90af2b72026-08-18WarningsExact identifier
application number: M032
EVERYDAY CLEAN DANDRUFFPYRITHIONE ZINCUniversal Distribution Center LLC3983b688-28ae-462e-8686-6cf2f2c1cca42026-08-18WarningsExact identifier
application number: M032
Prosoria Psoriasis TreatmentSALICYLIC ACIDNuvothera, Inc.378311aa-95f7-4c69-bc00-e688468262bd2026-08-18WarningsExact identifier
application number: M032
RoyceDerm Seborrheic Dermatitis and Psoriasis Treatment creamSALICYLIC ACID 3%RoyceDerm LLC496e178b-e29b-071e-e063-6394a90aa0182026-08-13WarningsExact identifier
application number: M032
RoyceDerm Seborrheic Dermatitis and Psoriasis shampoo.SALICYLIC ACID 3%RoyceDerm LLC4995ce33-e231-8f86-e063-6394a90af4862026-08-13WarningsExact identifier
application number: M032
Rida Hair Research Institute RHRI Neoketramin Antifungal Yeast ReliefPYRITHIONE ZINCRida LLCd1e4dee7-5962-4ec1-ab99-9d547077b2f22026-08-05WarningsExact identifier
application number: M032
Rida Hair Research Institute RHRI Neoketramin Antifungal Yeast Relief TreatmentSALICYLIC ACIDRida LLC6226ce12-432f-402e-bda7-a5ca96f0b8382026-08-05WarningsExact identifier
application number: M032
JOHNSON FOAMMINOXIDILJOHNSON BIOPHARMACEUTICAL INC.1d44a75c-c940-680c-e063-6394a90a58392026-08-02WarningsExact identifier
application number: M032
EVERYDAY CLEAN DANDRUFFPYRITHIONE ZINCNINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD.5a03d4bb-72e6-cc9f-e063-6394a90ae19f2026-08-01WarningsExact identifier
application number: M032
TEA TREE Oil DANDRUFFPYRITHIONE ZINCNINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD.5a0505a6-77ca-c56e-e063-6394a90aea6f2026-08-01WarningsExact identifier
application number: M032
ITCHY SCALP RELIEF DANDRUFFPYRITHIONE ZINCNINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD.5a0521cd-2b9e-e02c-e063-6394a90a5f022026-08-01WarningsExact identifier
application number: M032
SMOOTH AND SOFT DANDRUFFPYRITHIONE ZINCNINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD.5a054179-b0d7-3a0f-e063-6294a90a62092026-08-01WarningsExact identifier
application number: M032
FOLKI COSMETIC Psoriasis CreamSALICYLIC ACID 3% PSORIASIS CREAMWenzhou Yuyuan Pharmaceutical Co., Ltd.575786e0-21b8-ad9d-e063-6394a90ad0d42026-07-24WarningsExact identifier
application number: M032
RoyceDerm Psoriasis Scalp .spray.SALICYLIC ACID 2%RoyceDerm LLC57425b1a-4cf3-b133-e063-6394a90a84f52026-07-23WarningsExact identifier
application number: M032
RoyceDerm Psoriasis Scalp .Shampoo.SALICYLIC ACID 3%RoyceDerm LLC5743f813-57f7-f544-e063-6294a90ad3b82026-07-23WarningsExact identifier
application number: M032
Yodo SalilOINTMENTLaboratorio Neo Farmaco del Ecuador Neofarmaco Cia. LTDA.56812625-7eab-6a25-e063-6294a90a23fe2026-07-20WarningsExact identifier
application number: M032
Pureskin Seborrheic Dermatitis and Psoriasis CreamSEBORRHEIC DERMATITIS PSORIASIS CREAMBENLONG HALL LLC36086f7f-8536-417f-a302-37f78288489e2026-07-20WarningsExact identifier
application number: M032
5%MINOXIDIL TOPICAL FOAMMINOXIDILVeloce Trading Co., Limited56f87881-653f-17e6-e063-6294a90a67872026-07-19WarningsExact identifier
application number: M032
ProBliva Psoriasis Shampoo.SALICYLIC ACID 3%CAVTECH HOLDING LLC563e75f9-a1e2-2796-e063-6294a90aedb42026-07-10WarningsExact identifier
application number: M032
ProBliva Anti Dandruff Shampoo.SELENIUM SULFIDE 1%CAVTECH HOLDING LLC56022f6b-d7ba-1ccd-e063-6294a90a73102026-07-07WarningsExact identifier
application number: M032

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1245937zinc pyrithione 0.48 % Topical GelPSN1f7e0265-0543-4ef9-addf-4d514d0eedfe5
1245937zinc pyrithione 4.8 MG/ML Medicated ShampooSCD1f7e0265-0543-4ef9-addf-4d514d0eedfe5
1245937zinc pyrithione 0.48 % Topical GelSY1f7e0265-0543-4ef9-addf-4d514d0eedfe5

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
64724-1017-1647241017011 BOTTLE in 1 CARTON (64724-1017-1) / 150 mL in 1 BOTTLE1 bottle2012-02-290000-00-00NoNoCurrent