Spa Skilha
FDA Label NDC 66854-025

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 Spa Skilha (NDC 66854-025). 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.

Otc - Active Ingredient

Ethylhexyl methoxycinnamate, butyl methoxydibenzoylmethane, titanium dioxide and bis-ethylhexyl oxyphenol methoxyphenyl triazine offers total protection and wide spectrum against the UVA and UVB.

Otc - Purpose

As dermoprotective solar screen, moisturizes and nourishes. Delays photo-aging and prevents skin cancer.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children

Indications & Usage

Use this product when you exposed to the sun. SPF 40 UVA / UVB

Warnings

Avoid contact with eyes, do not use in the children under (6) six months of age.

Dosage & Administration

- Apply generously before sun exposure.- Reapply after (6) six hours.

Inactive Ingredient

Its composition is photo stable, perfectly adjusted to any state and any contidtion of the skin.

Package Label.Principal Display Panel

IMAGE OF THE LABELĀ 

Image Of The Label (Helioprotsfp40)

Image Of The Label (Helioprotsfp40)

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