Sulfur 8 Light Anti-dandruff Hair And Scalp Conditioner Ointment
FDA Label NDC 12022-018

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 Light Anti-dandruff Hair And Scalp Conditioner (NDC 12022-018). 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 ask a doctor if, if swallowed, get medical help or call a poison control center at once., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredients

Sulfur, 2%

Purpose

Antidandruff

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 Ask A Doctor If

  • condition worsens or does not improve after regular use.

If Swallowed, Get Medical Help Or Call A Poison Control Center At Once.

  • a gradual blue-black darking of the skin occurs
  • irritation becomes severe
  • no improvement is seen after 3 months

Directions

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

Inactive Ingredients

Petrolatum, Lanolin, Mineral Oil, Menthol, Fragrance, Yellow 11.

Package Labeling

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