Quality Choice Dandruff Everyday Clean

Manufacturer
CHAIN DRUG MARKETING ASSOCIATION, INC. | Medical Group Care LLC
Effective date
2025-01-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:53:34

Label at a glance#

ProductQuality Choice Dandruff Everyday Clean
Active ingredientPYRITHIONE ZINC
Label structure9 sections

Dosage and administration

shake before use wet hair, massage onto scalp, rinse and repeat if desired for best results use at least twice a week or as directed by a doctor for maximum dandruff control, use every time when you want to shampoo

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Pyrithione zinc

Purpose

OTC - PURPOSE SECTION

Antidandruff

Use

INDICATIONS & USAGE SECTION

helps prevent recurrence of scalp flaking and itching associated with dandruff.

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water

Stop use and ask a doctor if

OTC - STOP USE SECTION

condition worsens or does not improve after regular use of this product as directed

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

  • shake before use
  • wet hair, massage onto scalp, rinse and repeat if desired
  • for best results use at least twice a week or as directed by a doctor
  • for maximum dandruff control, use every time when you want to shampoo

Other information

OTHER SAFETY INFORMATION

store away from direct sunlight, excessive heat, and freezing conditions

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, sodium laureth sulfate, cocamidopropyl betaine, glycol distearate, acrylates copolymer, styrene/acrylates copolymer, polyquaternium-7, propylene glycol, sodium lauryl sulfate, cocamide MEA, phenoxyethanol, fragrance, sodium chloride, polyquaternium-10, ethylhexylglycerin, menthol, hydroxyacetophenone, FD&C blue no. 1, D&C red no. 33

Questions?

OTC - QUESTIONS SECTION

+1-800-935-2362
You may also report serious side effects to this phone number.

Monday-Friday 9AM-5PM EST

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

13 oz shampoo13 oz shampoo

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
209884zinc pyrithione 1 % Medicated ShampooPSN1
209884zinc pyrithione 10 MG/ML Medicated ShampooSCD1
209884zinc pyrithione 1 % Medicated ConditionerSY1
209884zinc pyrithione 1 % Medicated ShampooSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83324-320-13Quality Choice Dandruff Everyday Clean399 mL in 1 BOTTLE, PLASTICLOTION/SHAMPOO3991

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83324-320QUALITY CHOICE DANDRUFF EVERYDAY CLEAN (PYRITHIONE ZINC) LOTION/SHAMPOO [CHAIN DRUG MARKETING ASSOCIATION, INC.]1Current NDC, 1 package rows20250125_2c767d79-6ffe-ebaa-e063-6394a90a39d1.zip

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83324-32083324-320-13

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

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
Quality Choice Dandruff Everyday CleanPYRITHIONE ZINCCHAIN DRUG MARKETING ASSOCIATION, INC.2c767d79-6ffe-ebaa-e063-6394a90a39d12025-01-24WarningsExact identifier
ndc (package): 83324-320-13
ndc (product): 83324-320
ndc11 (package): 83324032013
spl id: 2c767d84-7efd-fc07-e063-6394a90a5a3c
spl set id: 2c767d79-6ffe-ebaa-e063-6394a90a39d1

Reported adverse events (FAERS/openFDA)#

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