Sulfur 8 Aqua Blue Shampoo, Suspension
FDA Label NDC 12022-024

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 Aqua Blue (NDC 12022-024). 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:, ask a doctor before use if you have, 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

Active Ingredients

Pyrithione Zinc, 1%

Purpose

Antidandruff

Use:

relieves scalp itching, irritation, redness, scaling and flaking associated with dandruff

Warnings:

For external use only

Ask A Doctor Before Use If You Have

  • seborrheic dermatitis that covers a large area of the body.

When Using This Product

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

Stop Use And Consult A Doctor If

  • conditions worsens or does not improve after regular use.

Keep Out Of Reach Of Children

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

Directions

  • shake well
  • for best results, use twice a week 
  • wet hair, apply shampoo, lather, rinse & repeat

Inactive Ingredients

SD Alcohol 40, Water, Propylene Glycol, Benzyl Alcohol, Menthol.

Package Labeling

12022-024-00 (12022 024 00)

12022-024-00 (12022 024 00)

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