Hampton Sun Spf 50 Mineral Spray
FDA Label NDC 87170-011

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by S&c Hampton Sun Llc for the product Hampton Sun Spf 50 Mineral (NDC 87170-011). 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 actove ingredeints                purpose, uses, warnings, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Actove Ingredeints                Purpose

Zinc Oxide 19.5%                     Sunscreen

Titanium Dioxide 4%               Sunscreen

Uses

Uses ■ helps prevent sunburn

Warnings

Warnings
For external use only.
Flammable: Do not use white smoking or near heat or flame.
Do not useon damaged or broken skin.
When using this product■ keep out of eyes. Rinse eyes with water
to remove.
Stop use and ask a doctor ifrash occurs.

Inactive Ingredients

Aloe Barbadensis Leaf Juice
Caprylic/Capric Triglyceride
Caprylyl Glycol
Cetyl Diglyceryl Tris(Trimethylsiloxy)silylethyl Dimethicone
Dimethicone
Ethylhexylglycerin
Fragrance
Glycerin
Hydrogen Dimethicone
Isopropyl Myristate
Jojoba Esters
Pentylene Glycol
Polyhydroxystearic Acid
Propanediol
Silica
Sodium Chloride
Sodium Hyaluronate
Sodium Phytate
Sorbitan Olivate
Stearic Acid
Synthetic Beeswax
Tocopheryl Acetate
Water

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