Panrosa Fresh Clean Pyrithione Zinc Dandruff
FDA Label NDC 50302-400

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Panrosa Enterprises, Inc. for the product Panrosa Fresh Clean Pyrithione Zinc Dandruff (NDC 50302-400). 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 active ingredient, purpose, use, warnings, when using this product, stop use and ask a doctor if, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Pyrithione zinc 1%

Purpose

Antidandruff

Use

helps prevent recurrence of flaking and itching
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.

Keep Out Of Reach Of Children.

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

Directions

  • Shake well
  • Wet hair
  • Massage shampoo into scalp
  • Rinse
  • Repeat if desired
  • For best results, use at least twice a week or as directed by a doctor
  • For maximum dandruff control, use every time you shampoo

Inactive Ingredients

Water, Sodium Larueth Sulfate, Ammonium Lauryl Sulfate, Cocamidopropyl Betaine, Cocamide MEA, Glycol Distearate, Dimethicone, Trideceth-5, Sodium Dodecylbenzenesulfonate, Sodium Chloride, Panthenol, Hydroxypropyl Guar, Cetearyl Alcohol, Fragrance, Allantoin, Disodium EDTA, Citric Acid, Methylchloroisothiazolinone, Methylisothiazolinone.

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