Head And Shoulders ®

Head And Shoulders ®
SPL v4
SPL
SPL Set ID c7bc3942-6943-2ea5-e053-2a95a90a42a9
Route
TOPICAL
Published
Effective Date 2020-12-16
Document Type 34390-5 HUMAN OTC DRUG LABEL

Drug Facts

Composition & Product

Active Ingredients
Pyrithione Zinc (0.75 g)
Inactive Ingredients
Methylchloroisothiazolinone Methylisothiazolinone Stearamidopropyl Dimethylamine Glutamic Acid Phenoxyethanol Benzyl Alcohol Citric Acid Monohydrate Honey Sodium Chloride Stearyl Alcohol Cetyl Alcohol Water Dimethicone

Identifiers & Packaging

Marketing Status
OTC MONOGRAPH DRUG Active Since 2021-01-11
Description

Drug Facts

Purpose

Anti-dandruff

Medication Information

Purpose

Anti-dandruff

Description

Drug Facts

Uses

helps prevent recurrence of flaking and itching associated with dandruff.

Section 42229-5

Drug Facts

Section 50565-1

Keep this and all drugs out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Warnings

For external use only.

Directions
  • for best results use at least twice a week or as directed by a doctor.
  • apply to wet hair after shampooing by gently massaging into hair and scalp, rinse well.
  • for maximum dandruff control, use every time you shampoo.
Active Ingredient

Pyrithione zinc .75%

Inactive Ingredients

Water, stearyl alcohol, cetyl alcohol, stearamidopropyl dimethylamine, glutamic acid, dimethicone, fragrance, phenoxyethanol, benzyl alcohol, sodium chloride, citric acid, honey extract,methylchloroisothiazolinone, methylisothiazolinone.

When Using This Product
  • avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.
Questions (or Comments)?

1-800-723-9569

Stop Use and Ask A Doctor If
  • condition worsens or does not improve after regular use of this product as directed.
Principal Display Panel Tube Label

head &

shoulders ®

pyrithione zinc dandruff conditioner

Clinical

Dandruff

Defense

Dry Scalp

Rescue

with Manuka Honey

100% DANDRUFF PROTECTION SATISFACTION GUARANTEED*

9.1 FL OZ (270 mL)

Structured Label Content

Uses

helps prevent recurrence of flaking and itching associated with dandruff.

Section 42229-5 (42229-5)

Drug Facts

Section 50565-1 (50565-1)

Keep this and all drugs out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Purpose

Anti-dandruff

Warnings

For external use only.

Directions
  • for best results use at least twice a week or as directed by a doctor.
  • apply to wet hair after shampooing by gently massaging into hair and scalp, rinse well.
  • for maximum dandruff control, use every time you shampoo.
Active Ingredient (Active ingredient)

Pyrithione zinc .75%

Inactive Ingredients (Inactive ingredients)

Water, stearyl alcohol, cetyl alcohol, stearamidopropyl dimethylamine, glutamic acid, dimethicone, fragrance, phenoxyethanol, benzyl alcohol, sodium chloride, citric acid, honey extract,methylchloroisothiazolinone, methylisothiazolinone.

When Using This Product (When using this product)
  • avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.
Questions (or Comments)? (Questions (or comments)?)

1-800-723-9569

Stop Use and Ask A Doctor If (Stop use and ask a doctor if)
  • condition worsens or does not improve after regular use of this product as directed.
Principal Display Panel Tube Label (PRINCIPAL DISPLAY PANEL - TUBE LABEL)

head &

shoulders ®

pyrithione zinc dandruff conditioner

Clinical

Dandruff

Defense

Dry Scalp

Rescue

with Manuka Honey

100% DANDRUFF PROTECTION SATISFACTION GUARANTEED*

9.1 FL OZ (270 mL)

Advanced Ingredient Data

Raw Label Data

All Sections (JSON)

Additional Information

Back to search View SPL set listing Open on DailyMed ↗

Source: dailymed · Ingested: 2026-02-15T12:07:48.393516 · Updated: 2026-03-14T23:11:37.729091