Otc - Active Ingredient
This product is an antibacterial liquid which produces a synergistic effect between the Triclosan is the active ingredient with a volatile carrier such as alcohol.
Dermaprot
FDA Label NDC 66854-013
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Spai-sons Pharmaceutical International Cosmetics for the product Dermaprot (NDC 66854-013). 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, warnings, dosage & administration, 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
This product is designed to produce an antibacterial effect both in the hands and utensils commonly used as combs and scissors in the facial aesthetics
Otc - Keep Out Of Reach Of Children
This product must be keep out of reach of children
Indications & Usage
This product is for topical application as well as being used in beauty salons utensils that need to be desinfected before being used.
Warnings
If this product to contact with eyes rinse immediately with water and consult a physician.
Dosage & Administration
Spray an hands before rubbing them.
Inactive Ingredient
The active ingredient is in a volatile carrier of alcohol, Aloe Vera extract and glycerin to help form a protective glove on the skin and objects that are using this product.
Package Label.Principal Display Panel
IMAGE OF THE LABEL
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