Head Remedy Dandruff Conditioner

Manufacturer
KPSS, Inc.
Effective date
2010-08-19
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:25:49

Label at a glance#

ProductHead Remedy Dandruff Conditioner
Active ingredientPYRITHIONE ZINC
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Zinc Pyrithione 1.0%

OTC - PURPOSE SECTION

Purpose: Antidandruff

INDICATIONS & USAGE SECTION

Use: Controls dandruff and flaking for a healthy scalp.

WARNINGS SECTION

Warnings: For external use only.

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have: seborrheic dermatitis that covers a large area of the body.

OTC - WHEN USING SECTION

When using this product: do not get in 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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep Out of Children's Reach: If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions: Apply small amount on shampooed hair. Massage into wet hair and scalp. Leave in 2 minutes and rinse. For best results, use at least 2 times a week.

OTC - QUESTIONS SECTION

Distributed by KPSS Inc., Linthicum Heights, MD 21090 USA, 1-800-342-5567

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of 8.5 fl oz labelImage of 8.5 fl oz labelMM1: 8oz_dandruff_conditioner_label.jpg

INACTIVE INGREDIENT SECTION

water, cetearyl alcohol, isopropyl palmitate, stearamidopropyl dimethylamine, phenethyl dimethicone, mineral oil, lactic acid, panthenol, butylene glycol, propylene glycol, glucose, Foeniculum vulgare (Fennel) fruit extract, Melissa officinalis (Balm) extract, Salvia officinalis (Sage) extract, Rosmarinus officinalis (Rosemary) extract, Urtica dioica (Nettle) extract, Equisetum arvense (Horsetail) extract, Humulus lupulus (Hops) extract, Chamomilla recutita (Matricaria) flower extract, caramel, sorbitol, sodium benzoate, potassium sorbate, DMDM Hydantoin, phenoxyethanol, tartaric acid, methylparaben, propylparaben, isobutylparaben, ethylparaben, butylparaben, fragrance, blue 1

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1043244head & shoulders 1 % Medicated ShampooPSN2
209884zinc pyrithione 1 % Medicated ShampooPSN2
1043244zinc pyrithione 10 MG/ML Medicated Shampoo [Head & Shoulders]SBD2
209884zinc pyrithione 10 MG/ML Medicated ShampooSCD2
1043244Head & Shoulders 1 % Medicated ShampooSY2
1043244Head & Shoulders 10 MG/ML Medicated ShampooSY2
209884zinc pyrithione 1 % Medicated ConditionerSY2
209884zinc pyrithione 1 % Medicated ShampooSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
25237-0516-12019-10-21C16284748780-1956f9ecf-d071-621f-e053-dbdaa90a74adDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
25237-0516-1Head Remedy Dandruff Conditioner249.4 g in 1 BOTTLEEMULSION249.42

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
25237-0516HEAD REMEDY DANDRUFF CONDITIONER (PYRITHIONE ZINC) EMULSION [KPSS, INC.]2Legacy NDC, 1 package rows20100915_2c00ade9-b7e7-4005-933a-bde9572cc437.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
PYRITHIONE ZINCACTIVE INGREDIENTR953O2RHZ52
PYRITHIONE ZINCACTIVE MOIETYR953O2RHZ52

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
25237-051625237-0516-1

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
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
c38bb28f-113e-48cb-8e52-509ccb9ecc092c00ade9-b7e7-4005-933a-bde9572cc4372010-08-19WarningsExact identifier
spl id: c38bb28f-113e-48cb-8e52-509ccb9ecc09
spl set id: 2c00ade9-b7e7-4005-933a-bde9572cc437

Reported adverse events (FAERS/openFDA)#

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