Sulfur 8 Scalp Therapy Medicated Dandruff Control Scalp Oil Serum Suspension
FDA Label NDC 12022-034

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 And Co. for the product Sulfur 8 Scalp Therapy Medicated Dandruff Control Scalp Oil Serum (NDC 12022-034). 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 consult 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

Sulfur, 2.5%

Purpose

Antidandruff

Use

Controls scalp itching an flaking due to 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 Consult A Doctor If

  • if skin irritation develops or increases.
  • condition worsens or does not improve after regular use as directed.

Keep Out Of Reach Of Children.

If swallowed, get medical help or call a Poison Control Center at once.

Hair is Flammable. Flammability is increased by proudct build-up. Keep hair away from sparks, flame, extreme heat or lit tobacco.

Directions

  • Shake well before using.
  • For best results, use at least twice a week, or as directed by a doctor.
  • Before shampooing your hair, apply a small amount to the scalp in several areas. Rub in well. Wait 15 minutes. Shampoo thoroughly.

Inactive Ingredients

Mineral Oil (Paraffinum Liquidum), Polysorbate 85, Disteardimonium Hectorite, Propylene Glycol, Benzyl Alcohol, Fragrance (Parfum)

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