Sulfur 8 Fresh Anti-dandruff Solution
FDA Label NDC 12022-028

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 Fresh Anti-dandruff (NDC 12022-028). 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.

Label Section Quick Index

Active Ingredients

Salicylic Acid, 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 Consult A Doctor If

  • condition 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 at once.

Directions

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

Inactive Ingredients

water, Mineral Oil, Aloe Barbadensis Leaf Juice, Isopropyl Myristate, Stearyl Alcohol, Ceteareth-20, Sodium Carbomer, Simmondsia Chinensis (Jojoba) Seed Oil, Hydrolyzed Collagen, Propylene Glycol, Tocopheryl Acetate, Methylparaben, Propylparaben, Diazolidinyl Urea, Sodium Lauryl Sulfate, Panthenol, Fragrance.

Package Labeling

12022-028-00 (12022 028 00)

12022-028-00 (12022 028 00)

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