Ouai Anti-dandruff Shampoo
FDA Label NDC 84126-905

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by The Procter & Gamble Manufacturing Company for the product Ouai Anti-dandruff (NDC 84126-905). 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 other, active ingredient, purpose, use, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Other

Drug Facts

DIST. BY OUAI BEVERLY HILLS,
CA 90210 USA

Active Ingredient

Salicylic Acid 2%

Purpose

Anti-Dandruff

Use

Reduces scalp flaking, itching, and irritation associated with dandruff

Warnings

For external use only

Directions

  • Apply to wet hair and massage into scalp.
  • Leave on for 5 minutes and rinse thoroughly.
  • For best results use at least twice a week or as directed by a doctor.

* Please review the disclaimer below.