Head & Shoulders Menthol Fresh

Head & Shoulders Menthol Fresh
SPL v1
SPL
SPL Set ID ffa115c5-c7b8-489a-b939-0004d36860fd
Route
TOPICAL
Published
Effective Date 2013-01-24
Document Type 34390-5 HUMAN OTC DRUG LABEL

Drug Facts

Composition & Product

Active Ingredients
Pyrithione Zinc (0.01 g)
Inactive Ingredients
Water Sodium Lauryl Sulfate Sodium Laureth Sulfate Glycol Distearate Zinc Carbonate Sodium Chloride Sodium Xylenesulfonate Dimethicone Cocamidopropyl Betaine Sodium Benzoate Magnesium Carbonate Hydroxide Methylchloroisothiazolinone Methylisothiazolinone Pyrithione Zinc Fd&c Blue No. 1 D&c Red No. 33

Identifiers & Packaging

Marketing Status
OTC MONOGRAPH FINAL Active Since 2013-01-24
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 43685-7

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.

Section 51945-4

Warnings

For external use only.

Directions
  • for best results use at least twice a week or as directed by a doctor.
  • for maximum dandruff control, use every time you shampoo.
  • wet hair, massage onto scalp, rinse, repeat if desired.
Active Ingredient

Pyrithione zinc 1%

Inactive Ingredients

Water, sodium lauryl sulfate, sodium laureth sulfate, glycol distearate, zinc carbonate, sodium chloride, fragrance, sodium xylenesulfonate, dimethicone, cocamidopropyl betaine, sodium benzoate, guar hydroxypropyltrimonium chloride, magnesium carbonate hydroxide, methylchloroisothiazolinone, methylisothiazolinone, pyrithione zinc, blue 1, red 33.

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

01-800-717-2413

Stop Use and Ask A Doctor If

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

Structured Label Content

Uses

helps prevent recurrence of flaking and itching associated with dandruff.

Section 43685-7 (43685-7)

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.

Section 51945-4 (51945-4)

Purpose

Anti-dandruff

Warnings

For external use only.

Directions
  • for best results use at least twice a week or as directed by a doctor.
  • for maximum dandruff control, use every time you shampoo.
  • wet hair, massage onto scalp, rinse, repeat if desired.
Active Ingredient (Active ingredient)

Pyrithione zinc 1%

Inactive Ingredients (Inactive ingredients)

Water, sodium lauryl sulfate, sodium laureth sulfate, glycol distearate, zinc carbonate, sodium chloride, fragrance, sodium xylenesulfonate, dimethicone, cocamidopropyl betaine, sodium benzoate, guar hydroxypropyltrimonium chloride, magnesium carbonate hydroxide, methylchloroisothiazolinone, methylisothiazolinone, pyrithione zinc, blue 1, red 33.

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)?)

01-800-717-2413

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.

Advanced Ingredient Data

Raw Label Data

All Sections (JSON)

Additional Information

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Source: dailymed · Ingested: 2026-02-15T11:55:34.772024 · Updated: 2026-03-14T22:53:23.299879