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OTC products · Product label record

Head and Shoulders Scalp Purify Volumizing drug information

SALICYLIC ACID
The Procter & Gamble Manufacturing Company · TOPICAL

Product NDC: 84126-908

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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 nameSALICYLIC ACID
Labeler / manufacturerThe Procter & Gamble Manufacturing Company
RouteTOPICAL
Drug classDrug class not supplied in source label
Product NDC84126-908
Label effective date2026-09-02

Official product label reference

Head and Shoulders Scalp Purify Volumizing — The Procter & Gamble Manufacturing Company

This page contains 11 source sections for SALICYLIC ACID, topical route. Label set 5a8627ec-cfd8-d0f6-e063-6394a90ab488, 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

Uses helps prevent recurrence of flaking and itching associated with dandruff

Purpose

Purpose Anti-Dandruff
Dosage and administration — label text
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 for 3 minutes, rinse, repeat if desired.
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 this and all drugs out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Unclassified section
Drug Facts DIST. BY PROCTER & GAMBLE, CINCINNATI, OH 45202
Active ingredient
Active Ingredient Salicylic Acid 1.8%
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 this and all drugs out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Inactive ingredient
Inactive Ingredients water, sodium laureth sulfate, sodium lauryl sulfate, sodium chloride, cocamidopropyl betaine, sodium xylenesulfonate, fragrance, sodium hydroxide, polyquaternium-10, citric acid, butylene glycol, piroctone olamine, glycerin, pentylene glycol, neosetophoma cerealis extract, menthol, niacinamide, sodium sulfite
Questions
Questions (or comments)? 1-800-723-9569

Official sources and product identifiers

Substances listed: SALICYLIC ACID

Package NDC codes

84126-908-40

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.