Sulfur 8 Scalp Therapy Medicated Dandruff Control Shampoo, Suspension
FDA Label NDC 12022-036
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 (NDC 12022-036). 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, ask a doctor before use if you have, when using this product, stop use and consult a doctor if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Pyrithione Zinc, 1%
Purpose
Antidandruff
Use
Controls scalp itching an flaking due to 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
avoid contact with 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 right away.
Directions
- shake well. for best results, use at least twice a week
- wet hair, apply shampoo. lather, rinse & repeat
Inactive Ingredients
Water, Ammonium Lauryl Sulfate, Propylene Glycol, Ammonium Laureth Sulfate, Cocamidopropyl Betaine, PEG-3 Glyceryl Cocoate, Hydroxypropyl Methylcellulose, Sodium Cocoamphopropionate, Glycol Distearate, Glycol Stearate, Glycol, Magnesium Aluminum Silicate, Benzyl Alcohol, Methylchloroisothiazolinone, Methylisothiazolinone, Triethylene Glycol, Magnesium Nitrate, Copper Sulfate, Citric Acid, Fragrance, Blue 1
Package Labeling:
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