Sulfur 8 Medicated Dandruff With Salicylic Acid Liquid
FDA Label NDC 12022-039
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by J. Strickland And Co. for the product Sulfur 8 Medicated Dandruff With Salicylic Acid (NDC 12022-039). 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, uses, warnings, ask a doctor before use, when using this product, stop use and ask a doctor, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Salicylic Acid, 2%
Purpose
Antidandruff, Seborrheic dermatitis, Psoriasis.
Uses
control the symptoms of
- dandruff
- seborrheic dermatitis
- psoriasis
Warnings
For external use only
Ask A Doctor Before Use
if you have
- a condition 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 Ask A Doctor
- if condition worsens or does not improve after regular use of this product as directed.
Keep Out Of Reach Of Children.
If swallowed, get medical help or call a Poison Control Center right away.
Directions
- For best results, use at least twice a week or as directed by a doctor.
- Apply a liberal amount of shampoo and massage into lather.
- Allow lather to remain on scalp for a few minutes.
- Rinse and repeat.
Inactive Ingrdients
Water, Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Betaine, Sodium Chloride, Polyquaternium-22, Menthol, Aloe Barbadensis Leaf Extract, PEG-40 Hydrogenated Castor Oil, Phenoxyethanol, Caprylyl Glycol, Ethylhexylglycerin, Disodium EDTA, Sodium Benzoate, Citric Acid, Potassium Sorbate, Sodium Sulfite, Sodium Hydroxide, Benzyl Benzoate, Fragrance.
Package Labeling:
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