Otc - Active Ingredient
Active Ingredient Purpose
Sulfur 10% ...................... ointment
Sulfur
FDA Label NDC 10095-007
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by World Perfumes, Inc for the product Sulfur (NDC 10095-007). 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 otc - active ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, dosage & administration, warnings, inactive ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Sulfur 10% ointment
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Indications & Usage
Sulfur 10% Ointment
Dosage & Administration
Sulfur 10% Ointment
Warnings
Sulfur 10% Ointment
Inactive Ingredient
cetyl/stearyl alcohol, glycerin, glyceryl stearate, methylparaben, mineral oil, paraffin, polyethylenglycol, propylparaben, sorbitan oleate, water
Package Label.Principal Display Panel
Label Image (Sulfur)
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