Sulfur 8 Original Anti-dandruff Hair And Scalp Conditioner Ointment
FDA Label NDC 12022-017

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 Original Anti-dandruff Hair And Scalp Conditioner (NDC 12022-017). 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

Sulfur, 2%

Purpose

Antidandruff

Use:

Controls scalp itching and flaking due to dandruff

Warnings:

For external use only

When Using This Product

  • Avoid contact with eyes. If contact occurs, rinse eyes throughly with water.

Stop Use And Ask A Doctor If

  • condition worsens or does not improve after regular use.

Keep Out Of Reach Of Children

If swallower, get medical help or call a poison control center at once.

Directions

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

Inactive Ingredients

Petrolatum, Landin, Sorbitan Trioleate, Pclysorbate 81, Menthol, Mineral Oil, Fragrance, Amyl Cinnamal, Cinnamal, Citral, Citronellol, Geraniol, Limonene, Linalool

Package Labeling

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