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Leader Classic Clean Dandruff drug information

PYRITHIONE ZINC
CARDINAL HEALTH 110, LLC. DBA LEADER · TOPICAL

Product NDC: 70000-0775

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Source label information, not individualized medical advice. This record applies to the product and labeler shown below. Compare the exact formulation, strength and country with your package and the current source label.
Generic namePYRITHIONE ZINC
Labeler / manufacturerCARDINAL HEALTH 110, LLC. DBA LEADER
RouteTOPICAL
Drug classDrug class not supplied in source label
Product NDC70000-0775
Label effective date2026-09-10

Official product label reference

Leader Classic Clean Dandruff — CARDINAL HEALTH 110, LLC. DBA LEADER

This page contains 12 source sections for PYRITHIONE ZINC, topical route. Label set 5b22537d-d09c-5bd6-e063-6294a90a48ff, version 1.

Retrieved 2026-10-02 · openFDA dataset updated 2026-10-02 · Check the current DailyMed label

Label records can cover multiple strengths or package sizes. A label listing does not by itself establish FDA approval or current market availability. Check the source and application history for this specific product.

Uses described in the label

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

Purpose

Purpose Antidandruff
Dosage and administration — label text
Directions 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
Warnings
Warnings For external use only When using this product avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water Stop use and ask a doctor if condition worsens or does not improve after regular use of this product as directed Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away
Unclassified section
Drug Facts
Active ingredient
Active Ingredient Pyrithione zinc
While using this medicine
When using this product avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water
When to stop use and seek help
Stop use and ask a doctor if condition worsens or does not improve after regular use of this product as directed
Child safety
Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away
Other safety information
Other information store away from direct sunlight, excessive heat, and freezing conditions
Inactive ingredient
Inactive ingredients 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
Questions? +1-866-306-9136 You may also report serious side effects to this phone number. Monday-Friday 9AM-5PM EST

Official sources and product identifiers

Substances listed: PYRITHIONE ZINC

RxNorm identifiers: 209884

Package NDC codes

70000-0775-1

Further research and background

These are external searches for related information. Research, encyclopedia and news articles have not been imported into this product record.

Coverage and corrections

The text is extracted from a US structured product label. Tables are represented as text where supplied; formatting and illustrations may be lost. A missing section does not mean a risk is absent. This reference has not been independently reviewed by a clinician and is not a live safety-alert service.

Source retrieved 2026-10-02. Read the source policy.