Moisturizing Sunscreen Spf15
FDA Label NDC 59663-001

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Shine & Pretty (usa), Corp. for the product Moisturizing Sunscreen Spf15 (NDC 59663-001). 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 - purpose, indications & usage, warnings, dosage & administration, inactive ingredient, otc - keep out of reach of children, otc - active ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Purpose

For Sun protection: Apply on surfaces of skin, on face, arm and hand. SPF-15 provides the face and body skin with effective protection against harmful UVA and UVB rays. Use daily over moisture cream to help prevent premature aging and wrinkling due to prolonged exposure to the sun, reapply after swimming or excessive exercise.

Indications & Usage

Smear Lightly.

Warnings

Warning: For external use only, not to be swallowed. Avoid contact with eye. Discontinue if signs of irritation or rash appear.

Dosage & Administration

To Apply lightly.

Inactive Ingredient

Inactive Ingredients: SORBITAN SESQUIOLEATE, POLYSORBATE 60, CARBOMER 934, VITAMIN E ACETATE, STEARIC ACID, PROPYLENE GLYCOL, VITAMIN A PALMITATE, PROPYLPARABEN, Water.

Otc - Keep Out Of Reach Of Children

Keep Out of the reach of children. Use on children under six months of age only with the advice of a physician.

Otc - Active Ingredient

OXYBENZONE and OCTINOXATE.

Package Label.Principal Display Panel

MM1

Label (Label2)

Label (Label2)

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