Active Ingredient
Salicylic Acid, 2%
Sulfur 8 Scalp Therapy Medicated Dandruff Control Spray
FDA Label NDC 12022-032
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 (NDC 12022-032). 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 ingredient, 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
Purpose
Antidandruff
Use:
Controls scalp itching and flaking due to dandruff
Warnings
For external use only
When Using This Product
avoid contact with eyes. If contact, rinse eyes thoroughly with water.
Stop Use And Consult 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 at once.
Directions
Spray to apply to the affected area 1-4 times daily, or as directed by a doctor
Inactive Ingredients
Water, Glycerin, Sodium Hydroxide, PEG-40 Hydrogenate Castor Oil, PEG-12 Dimethicone, Propylene Glycol, Hydrolyzed Collagen, Diazolidinyl Urea, Disodium EDT, Methylparaben, Propylparaben, Ethylhexylglycerin, PEG-12 Alyl Ether, PEG-12, Butylene Glycol, Phenoxyethanol, Fragrance
Package Labeling:
Image Description (Label)
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