FDA.reportPublic FDA data

J1002901Jason Dandruff Relief 2in1Treatment

Manufacturer
The Hain Celestial Group, Inc. | The Hain Celestial Group, Inc
Effective date
2021-04-12
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-05-31 23:39:36

Label at a glance#

ProductJ1002901Jason Dandruff Relief 2in1Treatment
Active ingredientPYRITHIONE ZINC
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Zinc Pyrithiopne 1.0%

OTC - PURPOSE SECTION

Controls Dandruff

INDICATIONS & USAGE SECTION

  • Controls recurrence of flaking, scaling and itching associated with dandruff
  • Helps prevent seborrheic dermatitis

WARNINGS SECTION

For external use only . Avoid contact with eyes.Rinse eyes throughly with water in case contact occurs.Discontinue use and consult your physician if irritation develops.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed get medical help or contact Poison Center right away.

DOSAGE & ADMINISTRATION SECTION

For best results use at least three times each week. Wet hair and lather, massage into scalp. Rinse and repeat if desired.

INACTIVE INGREDIENT SECTION

Water (Aqua), Sodium Cocoyl Isethionate, Cetyl Alcohol, Glycerin, Cocamidopropyl Hydroxysultaine, Sodium Laurylglucosides Hydroxypropylsulfonate, Sodium Cocoyl Glutamate, Sodium Chloride, Glyceryl Stearate SE, Coco-Glucoside, Glyceryl Oleate, Butyrospermum Parkii (Shea) Butter Unsaponifiables, Citrus Aurantium Dulcis (Orange) Peel Oil, Olea Europaea (Olive) Fruit Oil (1), Simmondsia Chinensis (Jojoba) Seed Oil (1), Soybean Glycerides, Chenopodium Quinoa Seed (1), Ascorbyl Palmitate, Babassu Oil Polyglyceryl-4 Esters, Benzyl Acetate, Caprylic/Capric Triglyceride, Capryloyl Glycerin/Sebacic Acid Copolymer, Cellulose Gum, Citric Acid, Diheptyl Succinate, Guar Hydroxypropyltrimonium Chloride, Phenethyl Alcohol, Sodium Hydroxide, Sodium PCA, Terpineol, Triethyl Citrate, Xanthan Gum, Zinc Carbonate, Alcohol (1), Ethylhexylglycerin, Phenoxyethanol, Potassium Sorbate, Limonene, Linalool.

(1) Certified Organic Ingredients

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

J10029 LabelJ10029 Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
209884zinc pyrithione 1 % Medicated ShampooPSN5
209884zinc pyrithione 10 MG/ML Medicated ShampooSCD5
209884zinc pyrithione 1 % Medicated ConditionerSY5
209884zinc pyrithione 1 % Medicated ShampooSY5

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
61995-0129-82023-01-30C16284748780-1ba0f9c33-3d8f-a910-e053-dadaa90a0b85Jason 2-in-1 Dandruff Shampoo & Conditioner
61995-0129-82021-02-05C16284748780-1ba0f9c33-3d8f-a910-e053-dadaa90a0b85Jason 2-in-1 Dandruff Shampoo & Conditioner
61995-0129-82021-01-29C16284748780-1ba0f9c33-3d8f-a910-e053-dadaa90a0b85Jason 2-in-1 Dandruff Shampoo & Conditioner

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61995-0129-8J1002901Jason Dandruff Relief 2in1Treatment355 g in 1 BOTTLESHAMPOO3555

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61995-0129J1002901JASON DANDRUFF RELIEF 2IN1TREATMENT (ZINC PYRITHIONE) SHAMPOO [THE HAIN CELESTIAL GROUP, INC.]5Legacy NDC, 1 package rows20210413_624c1961-57e2-79e5-e053-2991aa0aec27.zip

Products#

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

DailyMed product names page 1 of 1 · 40 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
61995-012961995-0129-8

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 38 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERYL OLEATE4PC054V79PIACT
SODIUM COCOYL GLUTAMATEBMT4RCZ3HGIACT
SODIUM DECYLGLUCOSIDES HYDROXYPROPYLSULFONATE55P9UXJ9C3IACT
SODIUM HYDROXIDE55X04QC32IIACT
TRIETHYL CITRATE8Z96QXD6UMIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
PHENOXYETHANOLHIE492ZZ3TIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
CAPRYLIC/CAPRIC ACIDDI775RT244IACT
OLIVE OIL6UYK2W1W1EIACT
CELLULOSE, MICROCRYSTALLINEOP1R32D61UIACT
GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE)B16G315W7AIACT
TERPINEOLR53Q4ZWC99IACT
XANTHAN GUMTTV12P4NEEIACT
STEARYL ALCOHOL2KR89I4H1YIACT
WATER059QF0KO0RIACT
SODIUM COCOYL ISETHIONATE518XTE8493IACT
GLYCERINPDC6A3C0OXIACT
CETYL ALCOHOL936JST6JCNIACT
BABASSU OIL8QSB4M5477IACT
JOJOBA OIL724GKU717MIACT
ZINC CARBONATEEQR32Y7H0MIACT
PYRITHIONE ZINCR953O2RHZ5ACTIB
DIHEPTYL SUCCINATE057N7SS26YIACT
ASCORBYL PALMITATEQN83US2B0NIACT
COCAMIDOPROPYL HYDROXYSULTAINE62V75NI93WIACT
SODIUM CHLORIDE451W47IQ8XIACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
ORANGE OILAKN3KSD11BIACT
GLYCERYL STEARATE SEFCZ5MH785IIACT
CHENOPODIUM QUINOA SEEDOO4K72NZ2XIACT
ALCOHOL3K9958V90MIACT
BENZYL ACETATE0ECG3V79ZJIACT
CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER (2000 MPA.S)N7YC58165TIACT
ORANGE PEELTI9T76XD44IACT
COCO GLUCOSIDEICS790225BIACT
SHEA BUTTERK49155WL9YIACT

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
bfc790c0-64fa-4ccd-e053-2995a90a2ecc624c1961-57e2-79e5-e053-2991aa0aec272021-04-12WarningsExact identifier
spl id: bfc790c0-64fa-4ccd-e053-2995a90a2ecc
spl set id: 624c1961-57e2-79e5-e053-2991aa0aec27

Reported adverse events (FAERS/openFDA)#

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