Suave Shampoo
FDA Label NDC 64942-1353

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Conopco Inc. D/b/a Unilever for the product Suave (NDC 64942-1353). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding otc - active ingredient, otc - purpose, indications & usage, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Active Ingredient

Active Ingredient

Pyrithione Zinc (1.0%)

Otc - Purpose

Purpose

Antidandruff

Indications & Usage

Use  controls scalp itching and flaking associated with dandruff.

Warnings

Warnings
For external use only

Otc - When Using

When using this product avoid contact with eyes.  If contact occurs, rinse eyes thoroughly with water.

Otc - Stop Use

Stop use and ask a doctor if condition worsens or does not improve after regular use of this product as directed.

Otc - Keep Out Of Reach Of Children

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

Dosage & Administration

Directions

• wet hair, lather, rinse, and repeat.

• for best results, use at least twice a week or as directed by a doctor.

Inactive Ingredient

Inactive Ingredients  Water (Aqua), Sodium Laureth Sulfate, Cocamidopropyl Betaine, Sodium Chloride, Fragrance (Parfum), Carbomer, Dimethiconol, DMDM Hydantoin, Citric Acid, Guar Hydroxypropyltrimonium Chloride, TEA-Dodecylbenzenesulfonate, Butylene Glycol, Propylene Glycol, Iodopropynyl Butylcarbamate, PPG-9, Methylchloroisothiazolinone, Methylisothiazolinone, Blue 1 (CI 42090).

Otc - Questions

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