Otc - Active Ingredient
ETHYLHEXYL METHOXYCINNAMATE, TITANIUM DIOXIDE, BUTYL METHOXYDIBENZOYLMETHANE, BENZOPHENONE-3, are a set of physical and chemical filters that provide SPF 30
Dermaprot
FDA Label NDC 66854-026
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 66854-026). 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
Sunscreen lotion from wide spectrum sunscreen SPF 30
Otc - Keep Out Of Reach Of Children
Keep out of reach of children
Indications & Usage
Provides moderate protection against sun. This product is for topical application.
Warnings
Avoid the contact with eyes, rinse with water to remove.
Do not apply this product on under six months aged children
Dosage & Administration
Rub to cover the area to be protected and wait for its full absorption
Inactive Ingredient
Solar protector UVA UVB has an aqeous base where we deposited all the active ingredients to garantee a wide range of the sun protection; rehydrates the skin tissues maintining cellular bioactivity without the inconvenient of the oily foundations.
Package Label.Principal Display Panel
IMAGE OF THE CARTON LABEL
Image Of The Carton Label (Helioprotsfp30)
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