Suave
FDA Label NDC 64942-2144

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 64942-2144). 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 drug facts, purpose, use, warnings, otc - keep out of reach of children, directions, inactive ingredients, questions/comments?, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Drug Facts

Active ingredient
Pyrithione Zinc (1.0%)

Purpose

Anti-dandruff

Use

Helps prevent and control recurrence of itching, flaking, redness and irritation associated with dandruff.

Warnings

For external use only


When using this product: avoid contact with 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.

Otc - Keep Out Of Reach Of Children

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

Directions

Shake before use.

For best results, use at least twice a week or as directed by a doctor.
Message into scalp and hair. Rinse

Inactive Ingredients

Water (Aqua), Sodium Laureth Sulfate, Cocamidopropyl Betaine, Sodium Chloride, Citric Acid, Carbomer, Dimethiconol, Phenoxyethanol, Fragrance (Parfum), Sodium Benzoate, Sodium Salicylate, PPG-9, Zinc Sulfate, Guar Hydroxypropyltrimonium Chloride, TEA-Dodecylbenzenesulfonate,

Questions/Comments?

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