Sulfur 8 Five Star Anti-dandruff Hair Groom Cream
FDA Label NDC 12022-030

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by J. Strickland & Co. for the product Sulfur 8 Five Star Anti-dandruff Hair Groom (NDC 12022-030). 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 ingredients, purpose, use:, warnings:, when using this product, stop use and consult 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.

Active Ingredients

Pyrithione Zinc, 0.1%

Purpose

Anti-dandruff

Use:

Controls scalp itching and flaking due to dandruff

Warnings:

For external use only

When Using This Product

  • do not get into eyes. If contact occurs, rinse eyes thoroughly with water.

Stop Use And Consult A Doctor If

  • condition worsens or does not improve after regular use.

Keep Out Of Reach Of Children

If swallowed, get medical helpor call a poison contril center at once.

Directions

  • Apply to the affected area 1-4 times daily, or as dircted by a doctor.

Inactive Ingredients

Water, Petrolatum, Mineral Oil, Glycerin, Ricinis Communis (Castor) Seed Oil, Stearyl Alcohol, Behentrimonium Methosulfate, Beeswax (Cera Alba), Dimethicone, Lanolin, Oleth-20, Polyquaterinium-11, Allantoin, Panthenol, Propylene Glycol, Butylene Glycol, Cetyl Alcohol, Sorbitan Trioleate, Diazolidinyl Urea, Methylparaben, Sodium Sulfate, Propylparaben, Fragrance (Parfum). 

Package Labeling

12022-030-00 (12022 030 00)

12022-030-00 (12022 030 00)

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