Control Dandruff Therapy Shampoo
FDA Label NDC 50718-0021

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Kamedis for the product Control Dandruff Therapy (NDC 50718-0021). 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, active ingredient, purpose, use, warnings, when using this product, stop use and ask a doctor if, keep out of reach of children, 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 eliminate scalp itching, irritation, redness, flaking, and scaling associated with dandruff

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

  • If condition worsens or does not improve after regular use of this product as directed, consult a doctor

Keep Out Of Reach Of Children

  • If swallowed, get medical help or contact a Poison Control Center right away

Directions

  • Apply to wet hair
  • Gently massage into hair and scalp and leave for 2-3 minutes before thoroughly rinsing
  • Rinse and repeat if desired
  • For best results use at least twice a week or as directed by your doctor

Inactive Ingredients

Ammonium Laureth Sulfate, Ammonium Lauryl Sulfate, Cocamidopropyl Betaine, Fragrance, Polyquaternium-10, Salicylic Acid, Salt(Sodium Chloride), Soapberry (Sapindus Mukurossi) Fruit Extract, Sodium Benzoate, Sodium Lauroyl Sarcosinate, Triethanolamine, Water.

Questions Or Comments?

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Carton Label

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